510(k) K053053 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
PACP SYSTEM
| Applicant | Pioneer Surgical Technology, Marquette MI, US |
| Decision | Substantially Equivalent, Nov 16, 2005 |
| Received | Oct 31, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K053053
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.