510(k) K102331 ยท MNI Orthosis, Spinal Pedicle Fixation
LDR SPINE USA SPINETUNE TL SPINAL SYSTEM
| Applicant | Ldr Spine USA, Austin TX, US |
| Decision | Substantially Equivalent, Oct 15, 2010 |
| Received | Aug 17, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K102331
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.