510(k) K032601 ยท GXD Generator, Lesion, Radiofrequency
STRYKER INTERVENTIONAL PAIN RF GENERATOR
| Applicant | Valley Forge Scientific Corp., Oaks PA, US |
| Decision | Substantially Equivalent, Apr 1, 2004 |
| Received | Aug 25, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032601
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 18, 2011 | Stryker Instruments Div. of Stryker Corporation Stryker Instruments, Interventional Spine RF MultiGen REF 0406-900-000, Rx only,, Stryker Instruments, Kalamazoo, MI (USA), 49001, (269) 323-7700, (800) 253-3210.
The product is intended for coagulati Terminated |
GXD | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.