S2 POSTERIOR-TIB — Anstek Corp. (510(k) K832296)
S2 POSTERIOR-TIB — Anstek Corp. (510(k) K832296) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: S2 POSTERIOR-TIB; Applicant: Anstek Corp.; Clearance track: 510(k).
| Device name | S2 POSTERIOR-TIB |
|---|---|
| Applicant | Anstek Corp. |
| Clearance track | 510(k) |
| Submission number | K832296 |
| Decision | Substantially Equivalent |
| Decision date | 1983-08-31 |
| Date received | 1983-07-13 |
| Product code | GXY |
| Device class | 2 |
| Medical specialty | Neurology |
| Applicant location | IL, US |
| Source | openFDA device |
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