510(k) K030241 ยท KWP Appliance, Fixation, Spinal Interlaminal
MODIFICATION TO BLACKSTONE SPINAL FIXATION SYSTEM
| Applicant | Blackstone Medical, Inc., Springfield MA, US |
| Decision | Substantially Equivalent, Feb 21, 2003 |
| Received | Jan 23, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K030241
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.