Genzyme Surgical Product (Genzyme Biosurgery) - FDA 510(k) Cleared De...
9
Total
8
Cleared
0
Denied
Genzyme Surgical Product (Genzyme Biosurgery) has 8 FDA 510(k) cleared medical devices. Based in Fall River, US.
Historical record: 8 cleared submissions from 1998 to 2000. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Genzyme Surgical Product (Genzyme Biosurgery) Filter by specialty or product code using the sidebar.
9 devices
Cleared
Nov 13, 2000
NEXTSTITCH CARDIOVASCULAR VALVE SUTURE
General & Plastic Surgery
189d
Cleared
Jun 12, 2000
'COTTONY' II DACRON, SILKY II POLYDEK & TEVDEK II POLYESTER NONABSORBABLE...
General & Plastic Surgery
35d
Cleared
Sep 03, 1999
BONDEK PLUS POLYGLYCOLIC ACID SYNTHETIC ABSORBABLE SURGICAL SUTURE
General & Plastic Surgery
74d
Cleared
Jul 20, 1999
ENDOSCOPIC CAMERA
General & Plastic Surgery
88d
Cleared
Jun 22, 1999
BONDEK POLYGLYCOLIC ACID SYNTHETIC ABSORBABLE SURGICAL SUTURE
General & Plastic Surgery
75d
Cleared
Mar 30, 1999
SAPHLIFT
General & Plastic Surgery
81d
Cleared
Dec 18, 1998
RAPID TRANSFER BLOOD BAG MODEL A-1650, RAPID TRANSFER BLOOD BAG MODEL S-250
Anesthesiology
136d
Cleared
Aug 07, 1998
MILLENNIUM VALVE INTRODUCER/ROTATOR HANDLE
Cardiovascular
217d
Cleared
Jul 07, 1998
CUTALON NYLON POLYAMIDE SURGICAL SUTURE
General & Plastic Surgery
88d