K-number	K053642
Device name	OSTEOSET DBM PELLETS
Applicant	Wrightmedicaltechnologyinc
Product code	MBP
Device class	Class II
Decision date	Jan 26, 2006
Decision	Substantially Equivalent
Regulation	888.3045

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Source

View the full FDA submission: accessdata.fda.gov

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OSTEOSET DBM PELLETS

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