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510k Database
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US
Biomet Corporation
Medical Device Manufacturer
·
US , Warsaw , IN
Biomet Corporation - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 2012
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Biomet Corporation
Orthopedic
✕
1
devices
1-1 of 1
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Cleared
Jul 26, 2012
COMPREHENSIVE REVERSE SHOULDER - E1 POLYETHYLENE CLAIMS
K121183
·
PHX
Orthopedic
·
99d
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Orthopedic
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