510(k) K052735 ยท MBP Filler, Bone Void, Osteoinduction (W/O Human Growth Factor)
ALLOCRAFT DBM
| Applicant | Lifecell Corp., Washington DC, US |
| Decision | Substantially Equivalent, Dec 28, 2005 |
| Received | Sep 30, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052735
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 26, 2008 | LifeCell Corporation AlloCraft DBM with Syringe Assembly, 5CC, Catalog/Reorder Number: 653005, LifeCell Corporation, Branchburg, NJ 08876 , Distributed by Stryker Spine Terminated |
MQV | None listed |
| Mar 26, 2008 | LifeCell Corporation AlloCraft DBM with Syringe Assembly, 10 CC, LifeCell Corporation, Branchburg, NJ 08876 , Distributed by Stryker Spine Terminated |
MQV | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.