COMPREHENSIVE CONVERTIBLE GLENOID — Biomet Manufacturing, Inc. (510(k) K130390)
COMPREHENSIVE CONVERTIBLE GLENOID — Biomet Manufacturing, Inc. (510(k) K130390) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: COMPREHENSIVE CONVERTIBLE GLENOID; Applicant: Biomet Manufacturing, Inc.; Clearance track: 510(k).
| Device name | COMPREHENSIVE CONVERTIBLE GLENOID |
|---|---|
| Applicant | Biomet Manufacturing, Inc. |
| Clearance track | 510(k) |
| Submission number | K130390 |
| Decision | Substantially Equivalent |
| Decision date | 2013-10-09 |
| Date received | 2013-02-15 |
| Product code | PHX |
| Device class | 2 |
| Medical specialty | Orthopedic |
| Applicant location | IN, US |
| Source | openFDA device |
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$1999/mo
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