K-number	K991854
Device name	OSTEOPLAST, MODEL POP200
Applicant	Interpore Cross Intl.
Product code	MQV
Device class	Class II
Decision date	Aug 26, 1999
Decision	Substantially Equivalent
Regulation	888.3045

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View the full FDA submission: accessdata.fda.gov

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OSTEOPLAST, MODEL POP200

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