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 |