Rebellion, Phantom Multi-Bite Kerrison Rongeur— 510(k) K230256

Name: FDA 510(k) clearance K230256
Creator: U.S. Food and Drug Administration
Published: 2023-03-03

Substantially Equivalent

Morpheus AG

FDA 510(k) clearance K230256 for Rebellion, Phantom Multi-Bite Kerrison Rongeur, Substantially Equivalent on 2023-03-03. Applicant: Morpheus AG. Device class: 2.

Clearance details

Applicant: Morpheus AG
Product code: Code HAE
Device class: Class 2
Regulation: 21 CFR 882.4840
Advisory panel: Neurology
Date received: 2023-01-31
Decision date: 2023-03-03
Decision: Substantially Equivalent
Clearance type: Special
Location: Spaichingen, DE

Download summary PDF View on FDA.gov ↗

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K200768 — Rebellion, Phantom Multi-Bite Kerrison Rongeur2021-05-04

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