510(k) K920392 ยท KWP Appliance, Fixation, Spinal Interlaminal
ISOLA SPINE SYSTEM: PLATE-ROD COMBINATION
| Applicant | Acromed Corp., Cleveland OH, US |
| Decision | Substantially Equivalent, Dec 31, 1992 |
| Received | Jan 30, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920392
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.