The following data is part of a premarket notification filed by Implanet, S.a. with the FDA for Madison Total Knee System.
Device ID | K192084 |
510k Number | K192084 |
Device Name: | Madison Total Knee System |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
Applicant | Implanet, S.A. Technopole Bordeaux Montesquieu, Allee Francois Magendie Martillac, FR 33650 |
Contact | Regis Le Couedic |
Correspondent | Hollace Saas Rhodes MCRA, LLC 1050 K Street NW, Suite 1000 Washington, DC 20001 |
Product Code | JWH |
CFR Regulation Number | 888.3560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-08-02 |
Decision Date | 2019-10-22 |
Summary: | summary |