ADG INTRAMEDULLARY BONE PLUG - VENTED— 510(k) K911717

Name: FDA 510(k) clearance K911717
Creator: U.S. Food and Drug Administration
Published: 1991-09-04

Substantially Equivalent

American Design Group, Inc.

FDA 510(k) clearance K911717 for ADG INTRAMEDULLARY BONE PLUG - VENTED, Substantially Equivalent on 1991-09-04. Applicant: American Design Group, Inc.. Device class: 2.

Clearance details

Applicant: American Design Group, Inc.
Product code: Code LZN
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 1991-04-17
Decision date: 1991-09-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Concord, CA, US

Download summary PDF View on FDA.gov ↗

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