510(k) K161279 ยท KWD Prosthesis, Toe, Hemi-, Phalangeal
Life Spine Metatarsal Hemi Implant
| Applicant | Life Spine, Inc., Huntley IL, US |
| Decision | Substantially Equivalent, Feb 1, 2017 |
| Received | May 6, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161279
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.