510(k) K150924 ยท GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)
A.I.M. Lead Loop Suturing Device (1), A.I.M. Tension Assist/Suture Cutter Device, A.I.M. Lead Loop Suturing Device (1) plus Tension Assist/Suture Cutter Device, A.I.M. Lead Loop Suturing Device (2), A.I.M. Lead Loop Suturing Device plus Tension Assist/Suture Cutter Device
| Applicant | Anchor Innovation Medical (A.I.M.), Rockville MD, US |
| Decision | Substantially Equivalent, Jul 27, 2015 |
| Received | Apr 6, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150924
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.