510(k) K061943 ยท KWP Appliance, Fixation, Spinal Interlaminal
ANATOMICA POSTERIOR CERVICAL FIXATION SYSTEM
| Applicant | Anatomica AB, Washington DC, US |
| Decision | Substantially Equivalent, May 25, 2007 |
| Received | Jul 10, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061943
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.