Medical Device Manufacturer · US , Edison , NJ

Musculoskeletal Transplant Foundation - FDA 510(k) Cleared Devices

24 submissions · 24 cleared · Since 2004

Recent clearances: MTF Pre-Sutured Tendon

24
Total
24
Cleared
0
Denied

Musculoskeletal Transplant Foundation has 24 FDA 510(k) cleared orthopedic devices. Based in Edison, US.

Historical record: 24 cleared submissions from 2004 to 2019.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Musculoskeletal Clinical Reulatory Advisers, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Musculoskeletal Transplant Foundation

24 devices
1-12 of 24
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