510(k) K981677 ยท LRK Device, Anti-Snoring
REPOSE BONE SCREW SYSTEM
| Applicant | Influence, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Aug 27, 1999 |
| Received | May 12, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981677
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Dec 15, 2009 | Medtronic Xomed, Inc. Repose G2 Bone Screw System, Sterile, REF 76353200; Lot # 62450300.
Distributed by Medtronic Xomed, Inc. Jacksonville, Florida 32216 U.S.A.
The Repose G@ Bone Screw System is composed of the Repose Terminated |
LRK | None listed |
| Dec 15, 2009 | Medtronic Xomed, Inc. Repose G2 Bone Screw, Sterile, REF 76310200, Lot # 62450200.
Distributed by Medtronic Xomed, Inc., Jacksonville, Florida 32216 U.S.A. Terminated |
LRK | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.