510(k) K050830 ยท KWP Appliance, Fixation, Spinal Interlaminal
ZODIAC SPINAL FIXATION SYSTEM
| Applicant | Alphatec/Nexmed, Carlsbad CA, US |
| Decision | Substantially Equivalent, Jun 22, 2005 |
| Received | Apr 1, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050830
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.