510(k) K132504 ยท KWP Appliance, Fixation, Spinal Interlaminal
TIGER OCCIPITAL-CERVICAL-THORACIC SPINAL FIXATION SYSTEM
| Applicant | Corelink, LLC, Washington DC, US |
| Decision | Substantially Equivalent, Nov 25, 2013 |
| Received | Aug 12, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132504
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.