Anthogyr INTEGRAL Guided Surgery Cassettes— 510(k) K233264

Name: FDA 510(k) clearance K233264
Creator: U.S. Food and Drug Administration
Published: 2023-12-22

Substantially Equivalent

Anthogyr

FDA 510(k) clearance K233264 for Anthogyr INTEGRAL Guided Surgery Cassettes, Substantially Equivalent on 2023-12-22. Applicant: Anthogyr. Device class: 2.

Clearance details

Applicant: Anthogyr
Product code: Code KCT
Device class: Class 2
Regulation: 21 CFR 880.6850
Advisory panel: General Hospital
Date received: 2023-09-29
Decision date: 2023-12-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sallanches, FR

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.