510(k) K101525 ยท KWP Appliance, Fixation, Spinal Interlaminal
PIONEER SPINOUS PROCESS FUSION PLATE
| Applicant | Pioneer Surgical Technology, West Newbury MA, US |
| Decision | Substantially Equivalent, Oct 22, 2010 |
| Received | Jun 2, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101525
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.