510(k) K172536 ยท LXM Manipulator, Plunger-Like Joint
Atlas Percussion Adjusting Instrument
| Applicant | Spinalight, Inc., St. Petersburg FL, US |
| Decision | Substantially Equivalent, Jun 20, 2018 |
| Received | Aug 22, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172536
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.