Johnson & Johnson Orthopaedics, Inc.
Johnson & Johnson Orthopaedics, Inc. holds FDA 510(k) medical device clearances, first cleared 1990, most recent 1994.
Top product codes for Johnson & Johnson Orthopaedics, Inc.
Recent clearances by Johnson & Johnson Orthopaedics, Inc.
- K931466 — PFC MODULAR TOTAL KNEE SYSTEM, POROUS COATED SACRI
- K935452 — P.F.C. 2 TOTAL HIP SYSTEM POROUS COATED MODULAR FEMORAL COMPONENT
- K940190 — ULTIMA UNIPOLAR MODULAR HEAD
- K933275 — P.F.C. CERAMIC HIP HEAD
- K932595 — ORTHOSORB(TM) ABSORBABLE CEMENT RESTRICTOR
- K931655 — P.F.C. BIPOLAR HIP SYSTEM
- K933867 — UNIVERSAL INSET PATELLA
- K935262 — P.F.C. TOTAL KNEE SYSTEM OVAL PATELLA
- K931189 — P.F.C. TOTAL HIP SYSTEM POROUS COATED MODULAR ACET
- K924340 — P.F.C. MOD TOTAL KNEE/CONDYL 3 FEM COMP TIB INSERT
- K931054 — TRICK MODULAR KNEE TIBIAL TRAY-POROUS
- K930712 — P.F.C. TOTAL HIP SYSTEM POROUS COATED MODULAR
- K924379 — ULTIMA(TM) TOTAL HIP SYSTEM CEMENTED FEMORAL STEM
- K924984 — SPECIALIST(R) WALKER
- K924115 — ULTIMA ALL UHMWPE CEMENTED ACETABULAR CUPS
- K913629 — JOHNSON AND JOHNSON POWER SYSTEM
- K914439 — P.F.C.(TM) UNICONDYLAR KNEE SYST, POR COAT FEMORAL
- K910968 — P.F.C. UNICONDYLAR KNEE SYSTEM
- K904737 — GROSS HIP FEMORAL COMPONENT
- K910563 — P.F.C.(R) MODULAR KNEE SYST, STAB ALL-PLAST TIBIAL
- K904300 — INSET PATELLAR COMPONENT
- K902137 — P.F.C. HIP SYSTEM NON-POROUS ACETABULAR COMPONENT
Data sourced from openFDA. This site is unofficial and independent of the FDA.