510(k) K071859 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
STRYKER CROSSFIRE SYSTEM
| Applicant | Stryker Endoscopy, San Jose CA, US |
| Decision | Substantially Equivalent, Sep 20, 2007 |
| Received | Jul 5, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071859
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 21, 2011 | Stryker Endoscopy Stryker Endoscopy 3.55 MM Super 90 S-SERFAS Energy Probe; electrosurgical device. Model number: 279-351-300; Terminated |
GEI | None listed |
| Aug 9, 2010 | Stryker Endoscopy Crossfire Console, model number 475-000-000, Manufactured by Stryker Endoscopy San Jose
Medical device indicated for use in orthopedic and arthroscopic procedures for the knee, shoulder, ankle, elbow Terminated |
GEI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.