Medical Device Manufacturer · US , Warsaw , IN

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

32 submissions · 32 cleared · Since 1999
32
Total
32
Cleared
0
Denied

Biomet Manufacturing, Inc. has 32 FDA 510(k) cleared orthopedic devices. Based in Warsaw, US.

Historical record: 32 cleared submissions from 1999 to 2013.

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 Manufacturing, Inc.
32 devices
1-12 of 32
Cleared Oct 09, 2013
COMPREHENSIVE CONVERTIBLE GLENOID
K130390 · PHX
Orthopedic · 236d
Cleared May 18, 2012
METAL-ON-METAL HIP SYSTEMS-ADDITIONAL CONTRAINDICATIONS
K113271 · KWA
Orthopedic · 196d
Cleared Dec 16, 2011
COMPREHENSIVE REVERSE SHOULDER
K113121 · PHX
Orthopedic · 56d
Cleared Aug 15, 2008
HIPLOC COMPRESSION HIP SCREW
K080685 · JDO
Orthopedic · 157d
Cleared Jun 11, 2008
BIOMET SPORTS MEDICINE ANCHOR DEVICES AND ZIPLOOP CONSTRUCTS
K080088 · HWC
Orthopedic · 149d
Cleared Oct 23, 2007
BIOMET CABLE SYSTEM
K071271 · JDQ
Orthopedic · 169d
Cleared May 04, 2007
100KGY E-POLY ACETABULAR LINERS-ADDITIONAL PROFILES
K070399 · JDI
Orthopedic · 81d
Cleared Feb 02, 2007
TITANIUM REPICCI II UNICONDYLAR FEMORAL KNEE COMPONENTS COCR REPICCI II...
K063515 · HRY
Orthopedic · 73d
Cleared Sep 25, 2006
23 MM SINGLE-PEG PATELLA COMPONENT
K061340 · JWH
Orthopedic · 133d
Cleared Aug 21, 2006
VANGUARD ANATOMIC PATELLA GROOVE (APG) / VANGUARD V GROOVE
K061433 · MBH
Orthopedic · 89d
Cleared Aug 14, 2006
REGENEREX ULTRA POROUS CONSTRUCT-FEMORAL AND TIBIAL KNEE AUGMENTS
K053505 · MBH
Orthopedic · 241d
Cleared May 03, 2006
GENERATION 4 POLISHED FEMORAL HIP PROSTHESIS WITH PROXIMAL CEMENT SPACER
K052639 · JDI
Orthopedic · 219d
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