The following data is part of a premarket notification filed by Cutter Laboratories, Inc. with the FDA for Tavernetti-tennant.
| Device ID | K760744 |
| 510k Number | K760744 |
| Device Name: | TAVERNETTI-TENNANT |
| Classification | Prosthesis, Knee, Femorotibial, Semi-constrained, Cemented, Metal/polymer |
| Applicant | CUTTER LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HRY |
| CFR Regulation Number | 888.3530 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-09-30 |
| Decision Date | 1976-10-07 |