The following data is part of a premarket notification filed by Techfit Digital Surgery Inc. with the FDA for Affinity Proximal Tibia System.
| Device ID | K220199 |
| 510k Number | K220199 |
| Device Name: | AFFINITY Proximal Tibia System |
| Classification | Plate, Fixation, Bone |
| Applicant | Techfit Digital Surgery INC. 1511 Aviation Center Pkwy, Suite 220H Daytona Beach, FL 32114 |
| Contact | Leidy Johanna Toro-Gonzalez |
| Correspondent | Leidy Johanna Toro-Gonzalez Techfit Digital Surgery INC. 1511 Aviation Center Pkwy, Suite 220H Daytona Beach, FL 32114 |
| Product Code | HRS |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2022-01-24 |
| Decision Date | 2022-03-21 |