510(k) K170902 ยท NHI Stimulator, Nerve, Electrical, Percutaneous (Pens), For Pain Relief
Sprint System, Single Procedure Kit, Sprint System with Pad II, Single Procedure Kit, Sprint System, Multi-Procedure Kit, Sprint System, Sterile Components Kit, Sprint System, Stimulator Kit
| Applicant | Spr Therapeutics, LLC, Cleveland OH, US |
| Decision | Substantially Equivalent, Jun 26, 2017 |
| Received | Mar 28, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170902
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.