Biocomposites is now offering a new antibiotic ceramic spacer designed for use in hip, knee, and shoulder applications.
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GSO is pleased to announce that it now offers LINK products.
LINK specializes in advanced orthopedic implants engineered to be completely free of nickel, chromium, and cobalt. Purpose‑built for patients with metal hypersensitivities, these innovative solutions help minimize the risk of allergic reactions while maintaining exceptional performance. LINK’s comprehensive portfolio includes options for total knee arthroplasty and hip replacement, delivering a trusted alternative to traditional cobalt–chrome implants for the 10–20% of patients affected by metal allergies.
Joint dislocation is still a significant challenge in hip replacement. EMPHASYS Acetabular Solutions provides an enhanced ability to treat patients who are at high risk of dislocation1 via an acetabular system that is designed with uncompromising stability in mind.2
ATTUNE™ Cementless Fixed Bearing Knee with AFFIXIUM™ 3DP Technology and the ATTUNE Medial Stabilized Knee System are designed for more natural knee function
WARSAW, IN, March 16, 2022 – Today, Johnson & Johnson MedTech* announced that DePuy Synthes,** The Orthopaedics Company of Johnson & Johnson, is adding two new innovations to its kinematically advanced and proveni,ii,iii,iv,v,vi ATTUNE™ Knee portfolio: the ATTUNE™ Cementless Fixed Bearing Knee with AFFIXIUM™ 3DP Technology and the ATTUNE™ Medial Stabilized Knee System.
The INHANCE Shoulder System is a first-to-market, fully convertible shoulder arthroplasty system that provides an efficient and intuitive plan to help simplify the surgeon and operating room (OR) staff’s existing workflow.
Designed for hospitals as well as outpatient and ASC settings where economic value and operational efficiency are critical considerations.
Warsaw, IN – May 16, 2022 – Today, Johnson & Johnson MedTech* announced that the INHANCE™ Shoulder System from DePuy Synthes, the Orthopaedics Company of Johnson & Johnson,** has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for use in reverse total shoulder arthroplasty procedures. This clearance is in addition to the system’s already cleared use in anatomic shoulder arthroplasty and provides surgeons with interoperative flexibility.