The following data is part of a premarket notification filed by Kinos Medical with the FDA for Kinos Axiom Total Ankle System.
| Device ID | K192778 |
| 510k Number | K192778 |
| Device Name: | Kinos Axiom Total Ankle System |
| Classification | Prosthesis, Ankle, Semi-constrained, Cemented, Metal/polymer |
| Applicant | Kinos Medical 992 Old Eagle School Road Suite 907 Wayne, PA 19087 |
| Contact | Brian Garvey |
| Correspondent | Alyssa Schwartz Alyssa Schwartz 992 Old Eagle School Road Suite 907 Wayne, PA 19087 |
| Product Code | HSN |
| CFR Regulation Number | 888.3110 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2019-09-30 |
| Decision Date | 2020-06-30 |
| Summary: | summary |