K-number	K960711
Device name	ACUMED BONE GRAFT SYSTEM
Applicant	Acu Med, Inc.
Product code	KIJ
Device class	Class I
Decision date	May 7, 1996
Decision	Substantially Equivalent
Regulation	878.4820

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View the full FDA submission: accessdata.fda.gov

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ACUMED BONE GRAFT SYSTEM

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