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 |