ARTHROTEK INTERFERENCE SCREW — Biomet, Inc. (510(k) K982497)
ARTHROTEK INTERFERENCE SCREW — Biomet, Inc. (510(k) K982497) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: ARTHROTEK INTERFERENCE SCREW; Applicant: Biomet, Inc.; Clearance track: 510(k).
| Device name | ARTHROTEK INTERFERENCE SCREW |
|---|---|
| Applicant | Biomet, Inc. |
| Clearance track | 510(k) |
| Submission number | K982497 |
| Decision | Substantially Equivalent |
| Decision date | 1998-10-16 |
| Date received | 1998-07-20 |
| 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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