510(k) K791056 ยท HSZ Instrument, Surgical, Orthopedic, Pneumatic Powered & Accessory/Attachment
3M CEMENT REMOVER
| Applicant | 3M Company, White City OR, US |
| Decision | Substantially Equivalent, Jul 30, 1979 |
| Received | Jun 8, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K791056
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.