510(k) K141835 ยท MNI Orthosis, Spinal Pedicle Fixation
ROMEO POSTERIOR OSTEOSYNTHESIS SYSTEM PREBENT CROSS-CONNECTORS; PREBENT RODS
| Applicant | Spineart, Geneva, CH |
| Decision | Substantially Equivalent, Sep 10, 2014 |
| Received | Jul 7, 2014 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K141835
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.