Instrument kits— 510(k) K160730

Substantially Equivalent

Anthogyr

FDA 510(k) clearance K160730 for Instrument kits, Substantially Equivalent on 2017-04-27. 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: 2016-03-16
Decision date: 2017-04-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sallanches, FR

Download summary PDF View on FDA.gov ↗

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K230680 — Anthogyr Surgical Cassettes2023-07-11
K093894 — ANTHOGYR IMPULSION IMPLANTOLOGY CONTRA-ANGLE2010-03-03

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