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DELTA XTEND Reverse Shoulder System featuring Carl J. Basamania, MD

Procedural Library

46 resources

Video, 07:22

At the end of this video the learner should understand the surgical steps for a double row rotator cuff repair utilizing HEALIX ADVANCE™ for medial row fixation and HEALIX ADVANCE Knotless Anchors for lateral row fixation.

Video, 02:27

Indications~Norian Drillable is intended for bony voids or defects of the extremities and pelvis that are not intrinsic to the stability of the bony structure. These defects may be surgically created osseous defects or osseous defects created from traumatic injury to the bone. The product provides a bone void filler that resorbs and is replaced with bone during the healing process. Norian Drillable can be used as an adjunct to conventional rigid hardware fixation by supporting the bone fragments during the surgical procedure. Once the material has set, it acts as a temporary support medium and is not intended to provide structural support during the healing process. Norian Drillable is intended to be placed into bony voids either before or after final fixation.~Contraindications~The safety and effectiveness of this device for use in the spine has not been established.~Use of this device is contraindicated in the spine, including use in the pedicle, as this could be associated with leakage of the device material into the bloodstream, which could cause serious adverse events, including death and should not be used in the presence of active or suspected infection.~Norian Drillable is not for screw augmentation.~Norian Drillable is not for use in:~Patients with traumatic open injuries that are predisposed to infection~Stress bearing applications~Areas where adjacent bone is avascular, or is incapable of supporting or anchoring the implanted rigid fixation hardware~Patients with compromised health (e.g. abnormal calcium metabolism, metabolic bone disease, a recent local untreated infection, vascular or severe neurological disease, infection, immunologic deficiencies or systemic disorders) that result in poor wound healing or will result in tissue deterioration over the implant site~Patients who are skeletally immature~Vertebral compression fractures~Intra?articular space (i.e. material injected into the joint space)~Please refer to the package insert for a complete list of indications, contraindications, precautions and warnings.~For further information on DePuy Synthes products, please contact your local DePuy Synthes representative.

Video, 04:25

Indications~Norian Drillable is intended for bony voids or defects of the extremities and pelvis that are not intrinsic to the stability of the bony structure. These defects may be surgically created osseous defects or osseous defects created from traumatic injury to the bone. The product provides a bone void filler that resorbs and is replaced with bone during the healing process. Norian Drillable can be used as an adjunct to conventional rigid hardware fixation by supporting the bone fragments during the surgical procedure. Once the material has set, it acts as a temporary support medium and is not intended to provide structural support during the healing process. Norian Drillable is intended to be placed into bony voids either before or after final fixation.~Contraindications~The safety and effectiveness of this device for use in the spine has not been established.~Use of this device is contraindicated in the spine, including use in the pedicle, as this could be associated with leakage of the device material into the bloodstream, which could cause serious adverse events, including death and should not be used in the presence of active or suspected infection.~Norian Drillable is not for screw augmentation.~Norian Drillable is not for use in:~Patients with traumatic open injuries that are predisposed to infection~Stress bearing applications~Areas where adjacent bone is avascular, or is incapable of supporting or anchoring the implanted rigid fixation hardware~Patients with compromised health (e.g. abnormal calcium metabolism, metabolic bone disease, a recent local untreated infection, vascular or severe neurological disease, infection, immunologic deficiencies or systemic disorders) that result in poor wound healing or will result in tissue deterioration over the implant site~Patients who are skeletally immature~Vertebral compression fractures~Intra?articular space (i.e. material injected into the joint space)~Please refer to the package insert for a complete list of indications, contraindications, precautions and warnings.~For further information on DePuy Synthes products, please contact your local DePuy Synthes representative.~

Technique Guide

Demineralized Bone Matrix with Delivery System.

Technique Guide

Indications~Norian Drillable is intended for bony voids or defects of the extremities and pelvis that are not intrinsic to the stability of the bony structure. These defects may be surgically created osseous defects or osseous defects created from traumatic injury to the bone. The product provides a bone void filler that resorbs and is replaced with bone during the healing process. Norian Drillable can be used as an adjunct to conventional rigid hardware fixation by supporting the bone fragments during the surgical procedure. Once the material has set, it acts as a temporary support medium and is not intended to provide structural support during the healing process. Norian Drillable is intended to be placed into bony voids either before or after final fixation.~Contraindications~The safety and effectiveness of this device for use in the spine has not been established.~Use of this device is contraindicated in the spine, including use in the pedicle, as this could be associated with leakage of the device material into the bloodstream, which could cause serious adverse events, including death and should not be used in the presence of active or suspected infection.~Norian Drillable is not for screw augmentation.~Norian Drillable is not for use in:~Patients with traumatic open injuries that are predisposed to infection~Stress bearing applications~Areas where adjacent bone is avascular, or is incapable of supporting or anchoring the implanted rigid fixation hardware~Patients with compromised health (e.g. abnormal calcium metabolism, metabolic bone disease, a recent local untreated infection, vascular or severe neurological disease, infection, immunologic deficiencies or systemic disorders) that result in poor wound healing or will result in tissue deterioration over the implant site~Patients who are skeletally immature~Vertebral compression fractures~Intra?articular space (i.e. material injected into the joint space)~Please refer to the package insert for a complete list of indications, contraindications, precautions and warnings.~For further information on DePuy Synthes products, please contact your local DePuy Synthes representative.~

Technique Guide

Indications~Norian Drillable is intended for bony voids or defects of the extremities and pelvis that are not intrinsic to the stability of the bony structure. These defects may be surgically created osseous defects or osseous defects created from traumatic injury to the bone. The product provides a bone void filler that resorbs and is replaced with bone during the healing process. Norian Drillable can be used as an adjunct to conventional rigid hardware fixation by supporting the bone fragments during the surgical procedure. Once the material has set, it acts as a temporary support medium and is not intended to provide structural support during the healing process. Norian Drillable is intended to be placed into bony voids either before or after final fixation.~Contraindications~The safety and effectiveness of this device for use in the spine has not been established.~Use of this device is contraindicated in the spine, including use in the pedicle, as this could be associated with leakage of the device material into the bloodstream, which could cause serious adverse events, including death and should not be used in the presence of active or suspected infection.~Norian Drillable is not for screw augmentation.~Norian Drillable is not for use in:~Patients with traumatic open injuries that are predisposed to infection~Stress bearing applications~Areas where adjacent bone is avascular, or is incapable of supporting or anchoring the implanted rigid fixation hardware~Patients with compromised health (e.g. abnormal calcium metabolism, metabolic bone disease, a recent local untreated infection, vascular or severe neurological disease, infection, immunologic deficiencies or systemic disorders) that result in poor wound healing or will result in tissue deterioration over the implant site~Patients who are skeletally immature~Vertebral compression fractures~Intra?articular space (i.e. material injected into the joint space)~Please refer to the package insert for a complete list of indications, contraindications, precautions and warnings.~For further information on DePuy Synthes products, please contact your local DePuy Synthes representative.~

Video, 12:19

Dr. Amir Moinfar presents a Double Row Repair using Mitek Sports Medicine’s newest anchors.~

Video, 06:12

Dr. Mark Albritton demonstrates a PASTA repair using the HEALIX TRANSTEND™ Implant System on an overhead athlete with an anterior supraspinatus partial thickness tear greater than 50% of the tendon.~

Video, 07:48

The HEALIX TRANSTEND™ Implant System is a percutaneous solution for partial tears of the rotator cuff.~

Video, 03:08

Dr. William Ciccone presents a Subscapularis & RC Repair utilizing the HEALIX Anchor™ 3.4mm.

Video, 05:20

Dr. Paul Favorito utilizes DePuy Synthes Mitek Sports Medicie HEALIX ADVANCE™ Knotless Anchors on a lateral row fixation for a rotator cuff repair.

Video, 05:53

William J. Ciccone, MD demonstrates arthroscopic allograft patch augmentation for a recurrent rotator cuff tear.

Video, 13:21

Paul Favorito, M.D. demonstrates his Superior Capsule Reconstruction technique using PERMATAPE™ Suture, HEALIX ADVANCE™ Knotless Anchors and Gryphon(BR) Suture Anchors

Video, 15:37

At the end of this course, the learner will have an understanding of how to utilize the GLOBAL STEPTECH Anchor Peg Glenoid in the treatment of shoulder arthritis.

Video, 05:02

The Atraumatic Soft Tissue Liberator is a device that safely allows a surgeon to perform a suprascapular nerve release.~

Video, 04:21

Dr. William J. Ciccone II demonstrates surgical techniques for In Suprapectoral Situ Biceps Tenodesis using the DePuy Synthes Mitek Sports Medicine HEALIX ADVANCE™ Knotless Anchor.

Video, 06:57

Dr. Krieg provides insight into when a nail should be used for fixing a proximal humerus fracture.

Video, 16:51

This video demonstrates the fixation of a valgus impacted proximal humerus fracture using the reviews the approach, reduction and positioning of the plate.

Video, 01:01:27

The DELTA XTEND™ Reverse Shoulder System is a total semi-constrained shoulder arthroplasty that reverses the normal relationship between the scapular and humeral components, moving the scapulo-humeral joint center of rotation medially and inferiorly, increasing the deltoid lever arm as well as the deltoid tension and therefore allowing the muscles of the deltoid group to compensate for rotator cuff deficiency.~

Video, 06:10

The Atraumatic Soft Tissue Liberator is a device that safely allows a surgeon to perform a suprascapular nerve release.~

Video, 06:51

Dr. Shariff K. Bishai utilizes the DePuy Synthes Mitek Sports Medicine HEALIX TRANSTEND on a 25-year-old right hand dominant male who suffered anterior shoulder dislocation as well as enlarged hill sachs lesion.~

Video, 06:10

Suprascapular Nerve Release using the DePuy Synthes Mitek Sports Medicine Atraumatic Soft Tissue Liberator (ASTL).

Video, 07:47

An open approach to the latarjet. A cadaveric demonstration utilizing the new LATARJET EXPERIENCE implant and instrumentation system from DEPUY SYNTHES MITEK SPORTS MEDICINE.

Video, 02:47

This video demonstrates the technique for fixing a two-part proximal humerus fracture through an anterolateral incision.

Video, 11:22

A Novel Arthroscopic Technique With The Use of A Tibial Plafond Allograft For Posterior Glenoid Bone Loss: Featuring The Latarjet Experience Shoulder Instability System from DEPUY SYNTHES MITEK SPORTS MEDICINE.

Video, 02:19

This video demonstrates the technique for fixing proximal humerus fractures utilizing the 3.5 mm LCP® Periarticular Proximal Humerus Plate and the 3.5 mm LCP® Proximal Humerus Plate.

Video, 06:57

This video demonstrates how to fix simple and complex proximal humerus fractures utilizing multiple locking options with the MultiLoc® Proximal Humeral Nail.

Video, 04:38

Proximal Humerus Plate Instruments facilitate screw insertion in the proximal humerus, particularly in osteoporotic bone.~

Video, 20:41

Proximal Humerus Plate Instruments facilitate screw insertion in the proximal humerus, particularly in osteoporotic bone.~

Video, 06:25

William J. Ciccone, MD demonstrates Arthroscopic Bankart Reconstruction featuring: GRYPHON® BR Suture Anchor with PROKNOT™ Technology

Video, 07:24

Watch Dr. Chris Chuinard perform suprascapular nerve release procedure using the atraumatic soft tissue liberator.~

Video, 26:03

Video featuring Dr. Matt Ravenscroft from Warrington, United Kingdom demonstrating an all arthroscopic Latarjet using the Bristow-Latarjet Instability Shouder System.

Video, 06:47

The HEALIX TRANSTEND™ Implant System is a percutaneous solution for partial tears of the rotator cuff.~

Video, 00:56

This video demonstrates the insertion of a headless compression screw and reduction of bone fragments.~

Brochure

Beta-Tricalcium Phosphate ( ?-TCP) bone graft substitute.

Technique Guide

GLOBAL® STEPTECH® Anchor Peg Glenoid builds on the clinical history of the GLOBAL Anchor Peg Glenoid Shoulder System by incorporating elements, and PREMIERON® X-Linked Polyethylene to create a technologically advanced glenoid implant.~

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Last Updated Jul 20, 2018