510(k) K140787 ยท MNH Orthosis, Spondylolisthesis Spinal Fixation
PLS (POSTERIOR LUMBAR SYSTEM)
| Applicant | Sintea Plustek, LLC, Fr. Myers FL, US |
| Decision | Substantially Equivalent, May 30, 2014 |
| Received | Mar 31, 2014 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K140787
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.