Biomet Orthopedics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biomet Orthopedics, Inc. - FDA 510(k) Cleared Devices
34
Total
34
Cleared
0
Denied
Biomet Orthopedics, Inc. has 34 FDA 510(k) cleared orthopedic devices. Based in Warsaw, US.
Historical record: 34 cleared submissions from 2000 to 2008.
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 - Biomet Orthopedics, Inc.
34 devices
Cleared
Jun 17, 2008
E-POLY TIBIAL BEARINGS
Orthopedic
112d
Cleared
Jan 14, 2008
INNERVUE DIAGNOSTIC SCOPE SYSTEM
Orthopedic
97d
Cleared
Oct 12, 2007
ACID ETCHED LAG SCREWS
Orthopedic
190d
Cleared
Jun 30, 2004
LACTOSCREW SCREW ANCHOR
Orthopedic
254d
Cleared
Nov 20, 2003
CALCIGEN PSI BONE GRAFT SUBSTITUTE
Orthopedic
119d
Cleared
Feb 05, 2003
HA PMI FEMORAL HIP STEM
Orthopedic
30d
Cleared
Jan 09, 2003
PROPELLER HEAD SMALL CANNULATED SCREW SYSTEM
Orthopedic
29d
Cleared
Dec 13, 2002
COMPREHENSIVE HUMERAL FRACTURE SYSTEM
Orthopedic
88d
Cleared
Dec 11, 2002
PRESS-FIT HEAD RESURFACING DEVICE
Orthopedic
78d
Cleared
Nov 06, 2002
ARCPM 1050 RESIN-HIPS
Orthopedic
30d
Cleared
Oct 25, 2002
RINGLOC CONSTRAINED LINERS
Orthopedic
158d
Cleared
Oct 17, 2002
RX 90 FEMORAL STEM AND RX 90 LATERALIZED FEMORAL STEM
Orthopedic
30d