Johnson & Johnson Orthopaedics, Inc. is one of 5836 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Johnson & Johnson Orthopaedics, Inc. - FDA 510(k) Cleared Devices
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
22
Total
19
Cleared
0
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
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