MEDNEXT 1000 BONE DISSECTING SYSTEM— 510(k) K926547

Name: FDA 510(k) clearance K926547
Creator: U.S. Food and Drug Administration
Published: 1993-07-22

Substantially Equivalent

Mednext, Inc.

FDA 510(k) clearance K926547 for MEDNEXT 1000 BONE DISSECTING SYSTEM, Substantially Equivalent on 1993-07-22. Applicant: Mednext, Inc.. Device class: 1.

Clearance details

Applicant: Mednext, Inc.
Product code: Code HSZ
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1992-12-31
Decision date: 1993-07-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Point Beach, FL, US

Download summary PDF View on FDA.gov ↗

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