510(k) K882070 ยท KWP Appliance, Fixation, Spinal Interlaminal
LUMBAR IMPACTION SET AND BONE GRAFT IMPACTORS
| Applicant | Karlin Technology, Inc., Marina Del Rey CA, US |
| Decision | Substantially Equivalent, Jun 3, 1988 |
| Received | May 17, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882070
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.