Surgeon Controlled Arm— 510(k) K223673

Name: FDA 510(k) clearance K223673
Creator: U.S. Food and Drug Administration
Published: 2023-08-04

Substantially Equivalent

Levita Magnetics International Corp

FDA 510(k) clearance K223673 for Surgeon Controlled Arm, Substantially Equivalent on 2023-08-04. Applicant: Levita Magnetics International Corp. Device class: 2.

Clearance details

Applicant: Levita Magnetics International Corp
Product code: Code PNL
Device class: Class 2
Regulation: 21 CFR 878.4815
Advisory panel: General, Plastic Surgery
Date received: 2022-12-07
Decision date: 2023-08-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Menlo Park, CA, US

Download summary PDF View on FDA.gov ↗

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