Please provide your email address to receive an email when new articles are posted on . It is generally accepted that spinal fusion, in conjunction with decompression, produces better clinical ...

ORLANDO, Fla., Feb. 26, 2025 /PRNewswire/ -- ABANZA, a leader in advanced soft tissue repair solutions, is proud to announce that the U.S. Food and Drug Administration (FDA) has granted 510(k) ...

ALLENDALE, N.J., June 29, 2023 (GLOBE NEWSWIRE) -- Acuitive Technologies, Inc. (Acuitive) today announced the first surgical use of its Citrelock® ACL Tendon Fixation Device. The new ACL device ...

MAHWAH, N.J.--(BUSINESS WIRE)--Stryker’s Trauma & Extremities division has launched its Citrelock™ Tendon Fixation Device System. The new system provides surgeons a differentiated design via a tendon ...

Panther Orthopedics has won FDA approval for its implantable orthopedic fixation device. The 510(k) nod clears Panther to sell a device designed to deliver continuous compression during bone healing ...

We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com. Back to Healio DePuy Synthes announced it has launched ...

A case series found that skin-stretching external fixation devices coupled with negative pressure wound therapy was effective in treating large skin defects, suggesting that this method may be a ...

ALLENDALE, N.J., Sept. 27, 2023 (GLOBE NEWSWIRE) — Acuitive Technologies, Inc. (Acuitive) today announced the FDA 510(k) Clearance of CITRELOCK DUO Fixation Device for biceps tenodesis. The new ...

The U.S. FDA’s safety and performance-based pathway (SPBP) is intended as a leaner, meaner alternative to the conventional 510(k) pathway that would sidestep some of the presumed problems with the ...