Biomet, Inc. - FDA 510(k) Cleared Devices
440
Total
418
Cleared
0
Denied
FDA 510(k) cleared devices by Biomet, Inc. General Hospital ✕
10 devices
Cleared
Aug 27, 2014
PERFUSE PERCUTANEOUS DECOMPRESSION SYSTEM
General Hospital
57d
Cleared
Mar 12, 2010
COAXIAL APPLICATOR SYSTEM
General Hospital
274d
Cleared
Dec 06, 2007
CONTROLLED DELIVERY FOR OSTEOPLASTY (CDO SYSTEM) AND GRAFT PREPARATION SYSTEM
General Hospital
108d
Cleared
Jan 14, 2003
DHS DISPOSABLE HOOD SYSTEM
General Hospital
210d
Cleared
Jul 01, 2002
PCCS GRAFT DELIVERY SYSTEM
General Hospital
90d
Cleared
Feb 07, 2000
DISPOSABLE INFUSION PUMP KIT
General Hospital
76d
Cleared
Jul 27, 1990
CUT RESISTANT GLOVE LINER
General Hospital
43d
Cleared
Feb 28, 1978
BED BOARD
General Hospital
19d
Cleared
Feb 21, 1978
BANDAGE, ELASTIC
General Hospital
12d
Cleared
Feb 21, 1978
RESTRAINT, PROTECTIVE
General Hospital
12d