510(k) K133363 ยท PEK Spinous Process Plate
INTERBRIDGE INTERSPINOUS POSTERIOR FIXATION SYSTEM
| Applicant | Ldr Spine USA, Inc., Colorado Springs CO, US |
| Decision | Substantially Equivalent, Mar 7, 2014 |
| Received | Nov 1, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133363
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.