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FDA 510(k)

Anthogyr FlexiBase® titanium bases for Axiom® BL

K-Number: K231072 · 2024-01-04

ApplicantAnthogyr
Decision Date2024-01-04
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Anthogyr FlexiBase® titanium bases for Axiom® BL is a medical device manufactured by Anthogyr. It received FDA 510(k) clearance on 2024-01-04 under approval number K231072. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Anthogyr FlexiBase® titanium bases for Axiom® BL?

Anthogyr FlexiBase® titanium bases for Axiom® BL is a medical device that received FDA 510(k) clearance on 2024-01-04. It is manufactured by Anthogyr. The 510(k) number is K231072.

When was Anthogyr FlexiBase® titanium bases for Axiom® BL approved by the FDA?

Anthogyr FlexiBase® titanium bases for Axiom® BL received FDA 510(k) clearance on 2024-01-04, under approval number K231072.

What company makes Anthogyr FlexiBase® titanium bases for Axiom® BL?

Anthogyr FlexiBase® titanium bases for Axiom® BL is manufactured by Anthogyr.

What is the FDA product code for Anthogyr FlexiBase® titanium bases for Axiom® BL?

The FDA product code for Anthogyr FlexiBase® titanium bases for Axiom® BL is NHA.

Other Devices by Anthogyr

K160730Instrument kits K233264Anthogyr INTEGRAL Guided Surgery Cassettes K230104Anthogyr AXIOM® BL X3 implants, Anthogyr Multi-Unit components for AXIOM® BL K230680Anthogyr Surgical Cassettes

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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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