The following data is part of a premarket notification filed by Howmedica Osteonics Corp with the FDA for Triathlon Ts Knee System.
Device ID | K070095 |
510k Number | K070095 |
Device Name: | 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 | 2007-01-10 |
Decision Date | 2007-06-01 |
Summary: | summary |