FDA 510(k)

Anthogyr INTEGRAL Guided Surgery Cassettes

K-Number: K233264 · 2023-12-22

Decision Date2023-12-22

Product CodeKCT

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

Anthogyr INTEGRAL Guided Surgery Cassettes is a medical device manufactured by Anthogyr. It received FDA 510(k) clearance on 2023-12-22 under approval number K233264. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Anthogyr INTEGRAL Guided Surgery Cassettes?

Anthogyr INTEGRAL Guided Surgery Cassettes is a medical device that received FDA 510(k) clearance on 2023-12-22. It is manufactured by Anthogyr. The 510(k) number is K233264.

When was Anthogyr INTEGRAL Guided Surgery Cassettes approved by the FDA?

Anthogyr INTEGRAL Guided Surgery Cassettes received FDA 510(k) clearance on 2023-12-22, under approval number K233264.

What company makes Anthogyr INTEGRAL Guided Surgery Cassettes?

Anthogyr INTEGRAL Guided Surgery Cassettes is manufactured by Anthogyr.

What is the FDA product code for Anthogyr INTEGRAL Guided Surgery Cassettes?

The FDA product code for Anthogyr INTEGRAL Guided Surgery Cassettes is KCT.

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Other Devices by Anthogyr

K160730Instrument kits K230104Anthogyr AXIOM® BL X3 implants, Anthogyr Multi-Unit components for AXIOM® BL K230680Anthogyr Surgical Cassettes K231072Anthogyr FlexiBase® titanium bases for Axiom® BL

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Official Source

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