510(k) K875290 ยท KWP Appliance, Fixation, Spinal Interlaminal
LUMBAR IMPACTION SET
| Applicant | T. Korossurgical Instruments Corp., Moorepark CA, US |
| Decision | Substantially Equivalent, Mar 4, 1988 |
| Received | Dec 30, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K875290
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.