510(k) K133374 ยท KWP Appliance, Fixation, Spinal Interlaminal
STREAMLINE OCT OCCIPITO-CERVICO-THORACIC SYSTEM
| Applicant | Pioneer Surgical Technology, Inc. (Rti Surgical, I, Marquette MI, US |
| Decision | Substantially Equivalent, Mar 19, 2014 |
| Received | Nov 1, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133374
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.