Episurf Medical Gains FDA Approval for IDE Study
Episurf Medical received FDA approval for its IDE application to commence a clinical study of the Episealer® knee device....
Episurf Medical received FDA approval for its IDE application to commence a clinical study of the Episealer® knee device....
Kinamed, developer of the CarboJet® CO2 bone prep system, announced a clinical study examining its use in traditional tourniquet vs. tourniquetless TKR....
Rejoint successfully completed mechanical testing of YourKnee, a TKA system that is additively manufactured in cobalt chrome. Limited launch is...
LimaCorporate has grown its SMR Shoulder system with launch of the SMR TT Hybrid Glenoid component....
United Orthopedic received FDA 510(k) clearance to market the E-XPEÂ vitamin E highly cross-linked polyethylene-based hip liner....
Integra LifeSciences launched the Integra® XT Revision Total Ankle Replacement system....
New clinical evidence represents positive mid-term survivorship results on 2,059 patients with Smith & Nephew's JOURNEY II BCS knee....
BioPoly received FDA approval to conduct an IDE clinical study of the BioPoly® RS Partial Resurfacing Knee....
Shoulder Innovations received FDA 510(k) clearance to market the InSet Humeral Short Stem....
Medacta received FDA 510(k) clearance to market the GMK® Sphere “ Kinematic Alignment surgical technique and technique-specific instruments for total knee arthroplasty....
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