510(k) K141508 ยท PEK Spinous Process Plate
ROMEO 2 PAD POSTERIOR AXIAL DEVICE
| Applicant | Spineart, Geneva, CH |
| Decision | Substantially Equivalent, Aug 21, 2014 |
| Received | Jun 6, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141508
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.