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 |