Medical Device Manufacturer · US , Braintree , MA

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

22 submissions · 19 cleared · Since 1990

22

Total

19

Cleared

0

Denied

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

21 devices

1-12 of 21

Cleared Dec 06, 1994

PFC MODULAR TOTAL KNEE SYSTEM, POROUS COATED SACRI

Orthopedic · 622d

Cleared Oct 06, 1994

P.F.C. 2 TOTAL HIP SYSTEM POROUS COATED MODULAR FEMORAL COMPONENT

Orthopedic · 328d

Cleared Sep 29, 1994

ULTIMA UNIPOLAR MODULAR HEAD

Orthopedic · 259d

Cleared Sep 28, 1994

P.F.C. CERAMIC HIP HEAD

Orthopedic · 449d

Cleared Sep 20, 1994

ORTHOSORB(TM) ABSORBABLE CEMENT RESTRICTOR

Orthopedic · 480d

Cleared Jun 09, 1994

P.F.C. BIPOLAR HIP SYSTEM

Orthopedic · 430d

Cleared Jun 06, 1994

UNIVERSAL INSET PATELLA

Orthopedic · 301d

Cleared Jun 03, 1994

P.F.C. TOTAL KNEE SYSTEM OVAL PATELLA

Orthopedic · 212d

Cleared Feb 09, 1994

P.F.C. TOTAL HIP SYSTEM POROUS COATED MODULAR ACET

Orthopedic · 337d

Cleared Jan 25, 1994

P.F.C. MOD TOTAL KNEE/CONDYL 3 FEM COMP TIB INSERT

Orthopedic · 515d

Cleared Jan 25, 1994

TRICK MODULAR KNEE TIBIAL TRAY-POROUS

Orthopedic · 330d

Cleared Oct 04, 1993

P.F.C. TOTAL HIP SYSTEM POROUS COATED MODULAR

Orthopedic · 235d