510(k) K001476 ยท LXM Manipulator, Plunger-Like Joint
TORQUE INSTRUMENT, MODEL 8500
| Applicant | Spinalight, Inc., Kennesaw GA, US |
| Decision | Substantially Equivalent, Aug 4, 2000 |
| Received | May 11, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001476
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.