Medical Device Manufacturer · US , Warsaw , IN

Biomet Orthopedics, Inc. - FDA 510(k) Cleared Devices

34 submissions · 34 cleared · Since 2000
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
1-12 of 34
Cleared Jun 17, 2008
E-POLY TIBIAL BEARINGS
K080528 · JWH
Orthopedic · 112d
Cleared Jan 14, 2008
INNERVUE DIAGNOSTIC SCOPE SYSTEM
K072879 · HRX
Orthopedic · 97d
Cleared Oct 12, 2007
ACID ETCHED LAG SCREWS
K070955 · HSB
Orthopedic · 190d
Cleared Jun 30, 2004
LACTOSCREW SCREW ANCHOR
K033355 · HWC
Orthopedic · 254d
Cleared Nov 20, 2003
CALCIGEN PSI BONE GRAFT SUBSTITUTE
K032286 · MQV
Orthopedic · 119d
Cleared Feb 05, 2003
HA PMI FEMORAL HIP STEM
K030048 · LPH
Orthopedic · 30d
Cleared Jan 09, 2003
PROPELLER HEAD SMALL CANNULATED SCREW SYSTEM
K024086 · HWC
Orthopedic · 29d
Cleared Dec 13, 2002
COMPREHENSIVE HUMERAL FRACTURE SYSTEM
K023063 · KWT
Orthopedic · 88d
Cleared Dec 11, 2002
PRESS-FIT HEAD RESURFACING DEVICE
K023188 · KXA
Orthopedic · 78d
Cleared Nov 06, 2002
ARCPM 1050 RESIN-HIPS
K023357 · LPH
Orthopedic · 30d
Cleared Oct 25, 2002
RINGLOC CONSTRAINED LINERS
K021661 · KWZ
Orthopedic · 158d
Cleared Oct 17, 2002
RX 90 FEMORAL STEM AND RX 90 LATERALIZED FEMORAL STEM
K023085 · JDI
Orthopedic · 30d
Filters
Filter by Specialty
All34 Orthopedic 34