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FDA 510(k)

TECHFIT DISRP® System

K-Number: K230276 · 2023-06-23

ApplicantTechfit Digital Surgery
Decision Date2023-06-23
Product CodeDZJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TECHFIT DISRP® System is a medical device manufactured by Techfit Digital Surgery. It received FDA 510(k) clearance on 2023-06-23 under approval number K230276. The device is classified under product code DZJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHFIT DISRP® System?

TECHFIT DISRP® System is a medical device that received FDA 510(k) clearance on 2023-06-23. It is manufactured by Techfit Digital Surgery. The 510(k) number is K230276.

When was TECHFIT DISRP® System approved by the FDA?

TECHFIT DISRP® System received FDA 510(k) clearance on 2023-06-23, under approval number K230276.

What company makes TECHFIT DISRP® System?

TECHFIT DISRP® System is manufactured by Techfit Digital Surgery.

What is the FDA product code for TECHFIT DISRP® System?

The FDA product code for TECHFIT DISRP® System is DZJ.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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