The following data is part of a premarket notification filed by Novosource Inc with the FDA for Tk1 Total Knee System.
Device ID | K123339 |
510k Number | K123339 |
Device Name: | TK1 TOTAL KNEE SYSTEM |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
Applicant | NOVOSOURCE INC 124 SOUTH 600 WEST Logan, UT 84321 |
Contact | James Pinkston |
Correspondent | James Pinkston NOVOSOURCE INC 124 SOUTH 600 WEST Logan, UT 84321 |
Product Code | JWH |
CFR Regulation Number | 888.3560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-10-31 |
Decision Date | 2013-04-11 |
Summary: | summary |