MediExpand Cervical Expandable VBR System— 510(k) K212126

Name: FDA 510(k) clearance K212126
Creator: U.S. Food and Drug Administration
Published: 2022-04-04

Substantially Equivalent

Cmf Medicon Surgical, Inc.

FDA 510(k) clearance K212126 for MediExpand Cervical Expandable VBR System, Substantially Equivalent on 2022-04-04. Applicant: Cmf Medicon Surgical, Inc.. Device class: 2.

Clearance details

Applicant: Cmf Medicon Surgical, Inc.
Product code: Code PLR
Device class: Class 2
Regulation: 21 CFR 888.3060
Advisory panel: Orthopedic
Date received: 2021-07-07
Decision date: 2022-04-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jacksonville, FL, US

Download summary PDF View on FDA.gov ↗

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