510(k) K073516 ยท BSP Needle, Conduction, Anesthetic (W/Wo Introducer)
DISCYPHOR DIRECT CATHETER SYSTEM, DISCYPHOR DIRECT NEEDLES, LONG, DISCYPHOR DIRECT NEEDLES, REGULAR
| Applicant | Kyphon, Inc., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Feb 21, 2008 |
| Received | Dec 14, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073516
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.