510(k) K001372 ยท KWP Appliance, Fixation, Spinal Interlaminal
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| Applicant | Depuyacromed, Raynham MA, US |
| Decision | Substantially Equivalent, Jul 27, 2000 |
| Received | May 1, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001372
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.