510(k) K043405 ยท MQP Spinal Vertebral Body Replacement Device
NUVASIVE COROENT SYSTEM
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Feb 7, 2005 |
| Received | Dec 10, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K043405
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 3, 2010 | Stryker Instruments Div. of Stryker Corporation Stryker Pain Pump 2 Luer Cap, REF 525-401, Rx, Sterile, Product of Ireland Manufactured for Stryker Instruments Kalamazoo MI Terminated |
FRN | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.