510(k) K002059 ยท KWP Appliance, Fixation, Spinal Interlaminal
AMT SPINAL SYSTEM
| Applicant | Micron Precision Engineering, Inc., San Pedro CA, US |
| Decision | Substantially Equivalent, Nov 13, 2000 |
| Received | Jul 6, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002059
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.