Comprehensive® Convertible Glenoid - Vivacit-E Liner — Biomet Manufacturing Corp (510(k) K211729)
Comprehensive® Convertible Glenoid - Vivacit-E Liner — Biomet Manufacturing Corp (510(k) K211729) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: Comprehensive® Convertible Glenoid - Vivacit-E Liner; Applicant: Biomet Manufacturing Corp; Clearance track: 510(k).
| Device name | Comprehensive® Convertible Glenoid - Vivacit-E Liner |
|---|---|
| Applicant | Biomet Manufacturing Corp |
| Clearance track | 510(k) |
| Submission number | K211729 |
| Decision | Substantially Equivalent |
| Decision date | 2021-11-04 |
| Date received | 2021-06-04 |
| 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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