510(k) K083663 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
PACP
| Applicant | Pioneer Surgical Technology, Marquette MI, US |
| Decision | Substantially Equivalent, Feb 25, 2009 |
| Received | Dec 10, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K083663
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.