K-number	K911717
Device name	ADG INTRAMEDULLARY BONE PLUG - VENTED
Applicant	American Design Group, Inc.
Product code	LZN
Device class	Class II
Decision date	Sep 4, 1991
Decision	Substantially Equivalent
Regulation	878.3300

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View the full FDA submission: accessdata.fda.gov

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ADG INTRAMEDULLARY BONE PLUG - VENTED

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