Howmedica Corp. - FDA 510(k) Cleared Devices
Recent clearances: MICRO DYNAMIC MESH, TYPE 3 FEMORAL COMPONENTS, DURATION II TIBIAL INSERTS-ETHYLENE OXIDE STERILIZATION
373
Total
325
Cleared
0
Denied
FDA 510(k) Regulatory Record - Howmedica Corp. General & Plastic Surgery ✕
7 devices
Cleared
Dec 30, 1983
DERMA STRIP-TM SKIN CLOSURES
General & Plastic Surgery
109d
Cleared
Jun 02, 1982
UNIFLEX
General & Plastic Surgery
100d
Cleared
May 14, 1982
DISP. SKIN STAPLER REMOVALBLE SKINSTAPLE
General & Plastic Surgery
31d
Cleared
May 14, 1982
DEKNATEL SKIN STAPLE EXTRACTOR
General & Plastic Surgery
17d
Cleared
Jan 15, 1981
BONE-DRI SURGICAL SPONGE
General & Plastic Surgery
34d
Cleared
Sep 26, 1980
GABBAY-FRATER SUTURE GUIDE
General & Plastic Surgery
24d
Cleared
Jan 12, 1978
INTERMEDULLARY BRUSH
General & Plastic Surgery
220d