AFFINITY Proximal Tibia System

Plate, Fixation, Bone

Techfit Digital Surgery INC.

The following data is part of a premarket notification filed by Techfit Digital Surgery Inc. with the FDA for Affinity Proximal Tibia System.

Pre-market Notification Details

Device IDK220199
510k NumberK220199
Device Name:AFFINITY Proximal Tibia System
ClassificationPlate, Fixation, Bone
Applicant Techfit Digital Surgery INC. 1511 Aviation Center Pkwy, Suite 220H Daytona Beach,  FL  32114
ContactLeidy Johanna Toro-Gonzalez
CorrespondentLeidy Johanna Toro-Gonzalez
Techfit Digital Surgery INC. 1511 Aviation Center Pkwy, Suite 220H Daytona Beach,  FL  32114
Product CodeHRS  
CFR Regulation Number888.3030 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2022-01-24
Decision Date2022-03-21

NIH GUDID Devices

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