ADG BONE PLUG— 510(k) K902615

Substantially Equivalent

American Design Group, Inc.

FDA 510(k) clearance K902615 for ADG BONE PLUG, Substantially Equivalent on 1990-09-11. 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: 1990-06-13
Decision date: 1990-09-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Concord, CA, US

Download summary PDF View on FDA.gov ↗

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More clearances from American Design Group, Inc.

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