The following data is part of a premarket notification filed by Corin Usa Limited with the FDA for Unity Total Knee System.
Device ID | K173884 |
510k Number | K173884 |
Device Name: | Unity Total Knee System |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
Applicant | Corin USA Limited 12750 Citrus Park Lane Tampa, FL 33625 |
Contact | Lorraine Mander |
Correspondent | Lorraine Mander Corin USA Limited 12750 Citrus Park Lane Tampa, FL 33625 |
Product Code | JWH |
CFR Regulation Number | 888.3560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-12-21 |
Decision Date | 2018-01-17 |
Summary: | summary |