510(k) K902002 ยท DTB Permanent Pacemaker Electrode
MODELS 5069/5071 MYOCARDIAL PACING LEADS
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Sep 26, 1990 |
| Received | May 2, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902002
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 23, 2010 | Medtronic Inc. Cardiac Rhythm Disease Managment Medtronic, Sutureless, unipolar, myocardial, screw-in pacing lead, 5071-15, 5071-25, 5071-35 & 5071-53, Medtronic, Inc., Minneapolis, MN 55432, Manufactured in: Villalba, Puerto Rico. Terminated |
DTB | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.