Medical Device Manufacturer · US , Braintree , MA

Johnson & Johnson Orthopaedics, Inc. - FDA 510(k) Cleared Devices

22 submissions · 19 cleared · Since 1990

Recent clearances: PFC MODULAR TOTAL KNEE SYSTEM, POROUS COATED SACRI, P.F.C. 2 TOTAL HIP SYSTEM POROUS COATED MODULAR FEMORAL COMPONENT, ULTIMA UNIPOLAR MODULAR HEAD

View 22 510(k) Devices ↓

22

Total

19

Cleared

0

Denied

FDA 510(k) Regulatory Record - Johnson & Johnson Orthopaedics, Inc. General Hospital ✕

1 devices

1-1 of 1

Cleared Feb 01, 1993

SPECIALIST(R) WALKER

General Hospital · 123d