Medical Device Manufacturer · US , Braintree , MA

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

22 submissions · 19 cleared · Since 1990

Total

Cleared

Denied

Johnson & Johnson Orthopaedics, Inc. has 19 FDA 510(k) cleared orthopedic devices. Based in Braintree, US.

Historical record: 19 cleared submissions from 1990 to 1994.

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

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

22 devices

1-12 of 22

Cleared Dec 06, 1994

PFC MODULAR TOTAL KNEE SYSTEM, POROUS COATED SACRI

K931466 · JWH

Orthopedic · 622d

Cleared Oct 06, 1994

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

K935452 · LZO

Orthopedic · 328d

Cleared Sep 29, 1994

ULTIMA UNIPOLAR MODULAR HEAD

K940190 · KWL

Orthopedic · 259d

Cleared Sep 28, 1994

P.F.C. CERAMIC HIP HEAD

K933275 · LZO

Orthopedic · 449d

Cleared Sep 20, 1994

ORTHOSORB(TM) ABSORBABLE CEMENT RESTRICTOR

K932595 · LZN

Orthopedic · 480d

Cleared Jun 09, 1994

P.F.C. BIPOLAR HIP SYSTEM

K931655 · KWY

Orthopedic · 430d

Cleared Jun 06, 1994

UNIVERSAL INSET PATELLA

K933867 · JWH

Orthopedic · 301d

Cleared Jun 03, 1994

P.F.C. TOTAL KNEE SYSTEM OVAL PATELLA

K935262 · JWH

Orthopedic · 212d

Cleared Feb 09, 1994

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

K931189 · LZO

Orthopedic · 337d

Cleared Jan 25, 1994

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

K924340 · JWH

Orthopedic · 515d

Cleared Jan 25, 1994

TRICK MODULAR KNEE TIBIAL TRAY-POROUS

K931054 · JWH

Orthopedic · 330d

Cleared Oct 04, 1993

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

K930712 · LZO

Orthopedic · 235d

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

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