FDA 510(k) Applications Submitted by BIOMET MANUFACTUTING CORP.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K123297 | 10/22/2012 | COMPRESS SEGMENTAL HUMERAL REPLACEMENT SYSTEM | BIOMET MANUFACTUTING CORP. |
| K142746 | 09/24/2014 | G7 Finned Acetabular Shell | BIOMET MANUFACTUTING CORP. |
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