The following data is part of a premarket notification filed by Howmedica Osteonics Corp with the FDA for Triathlon Press-fit Total Knee System.
Device ID | K051380 |
510k Number | K051380 |
Device Name: | TRIATHLON PRESS-FIT TOTAL KNEE SYSTEM |
Classification | Prosthesis, Knee, Patello/femorotibial, Semi-constrained, Uncemented, Porous, Coated, 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 | MBH |
CFR Regulation Number | 888.3565 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-05-27 |
Decision Date | 2005-08-30 |
Summary: | summary |