Johnson & Johnson International - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Johnson & Johnson International has 10 FDA 510(k) cleared medical devices. Based in New Brunswick, US.
Historical record: 10 cleared submissions from 1989 to 1997. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Johnson & Johnson International Filter by specialty or product code using the sidebar.
10 devices
Cleared
Jul 23, 1997
ULTIMA TPS CEMENTED STEM
Orthopedic
209d
Cleared
May 19, 1995
SYNTHETIC ABSORBABLE SUTURE
General & Plastic Surgery
225d
Cleared
Apr 11, 1995
TIELLE* HYDROPOLYMER DRESSING
General & Plastic Surgery
110d
Cleared
Aug 22, 1994
DERMIVIEW CLEAR TAPE
General & Plastic Surgery
95d
Cleared
Jul 06, 1993
BARRIER SAF-TE HYDROGEL DRAPE
General Hospital
383d
Cleared
Nov 09, 1992
P.F.C. MODULAR TOTAL KNEE SYSTEM, MODULAR PLUS
Orthopedic
103d
Cleared
Nov 21, 1990
BIOCLUSIVE(R) ABSORBENT DRESSING
General & Plastic Surgery
352d
Cleared
Aug 15, 1990
ORTHOSORB(R) ABSORBABLE PIN
Orthopedic
141d
Cleared
Apr 30, 1990
P.F.C. HIP SYSTEM NON-POROUS FEMORAL COMPONENT
Orthopedic
80d
Cleared
Sep 28, 1989
BIOCLUSIVE* TRANSPARENT FILM DRESSING - NEW CLAIM
General & Plastic Surgery
42d