510(k) K040417 ยท LRK Device, Anti-Snoring
PILLAR PALATAL IMPLANT SYSTEM
| Applicant | Restore Medical, Inc., Roseville MN, US |
| Decision | Substantially Equivalent, Jul 28, 2004 |
| Received | Feb 18, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K040417
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.