The following data is part of a premarket notification filed by Howmedica Osteonics Corp. with the FDA for Modification To Triathlon Ts Knee System.
| Device ID | K072221 |
| 510k Number | K072221 |
| Device Name: | MODIFICATION TO TRIATHLON TS KNEE SYSTEM |
| Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
| Applicant | HOWMEDICA OSTEONICS CORP. 325 CORPORATE DR Mahwah, NJ 07430 |
| Contact | Tiffani Rogers |
| Correspondent | Tiffani Rogers HOWMEDICA OSTEONICS CORP. 325 CORPORATE DR Mahwah, NJ 07430 |
| Product Code | JWH |
| CFR Regulation Number | 888.3560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-08-10 |
| Decision Date | 2007-10-15 |
| Summary: | summary |