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FDA 510(k)

Trax EX Anchor

K-Number: K251750 · 2026-03-12

ApplicantTrax Surgical, Inc.
Decision Date2026-03-12
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Trax EX Anchor is a medical device manufactured by Trax Surgical, Inc.. It received FDA 510(k) clearance on 2026-03-12 under approval number K251750. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Trax EX Anchor?

Trax EX Anchor is a medical device that received FDA 510(k) clearance on 2026-03-12. It is manufactured by Trax Surgical, Inc.. The 510(k) number is K251750.

When was Trax EX Anchor approved by the FDA?

Trax EX Anchor received FDA 510(k) clearance on 2026-03-12, under approval number K251750.

What company makes Trax EX Anchor?

Trax EX Anchor is manufactured by Trax Surgical, Inc..

What is the FDA product code for Trax EX Anchor?

The FDA product code for Trax EX Anchor is MBI.

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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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