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FDA 510(k)

Tactoset

K-Number: K223915 · 2023-03-29

ApplicantAnika Therapeutics, Inc.
Decision Date2023-03-29
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Tactoset is a medical device manufactured by Anika Therapeutics, Inc.. It received FDA 510(k) clearance on 2023-03-29 under approval number K223915. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Tactoset?

Tactoset is a medical device that received FDA 510(k) clearance on 2023-03-29. It is manufactured by Anika Therapeutics, Inc.. The 510(k) number is K223915.

When was Tactoset approved by the FDA?

Tactoset received FDA 510(k) clearance on 2023-03-29, under approval number K223915.

What company makes Tactoset?

Tactoset is manufactured by Anika Therapeutics, Inc..

What is the FDA product code for Tactoset?

The FDA product code for Tactoset is MQV.

Other Devices by Anika Therapeutics, Inc.

K173008SCS 17-01 K190956SCS 17-01 K212083Tactoset Injectable Bone Substitute K231968Tactoset® Injectable Bone Substitute K223538Integrity Implant K223860Integrity™ Bone Staple Fixation System

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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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