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 |