BONE MULCH SCREW — Biomet, Inc. (510(k) K941941)
BONE MULCH SCREW — Biomet, Inc. (510(k) K941941) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: BONE MULCH SCREW; Applicant: Biomet, Inc.; Clearance track: 510(k).
| Device name | BONE MULCH SCREW |
|---|---|
| Applicant | Biomet, Inc. |
| Clearance track | 510(k) |
| Submission number | K941941 |
| Decision | Substantially Equivalent for Some Indications |
| Decision date | 1995-02-02 |
| Date received | 1994-04-21 |
| Product code | HWC |
| Device class | 2 |
| Medical specialty | Orthopedic |
| Applicant location | IN, US |
| Source | openFDA device |
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$1999/mo
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