K-number	K122382
Device name	DYNASTY BIOFOAM SHELL
Applicant	Wrightmedicaltechnologyinc
Product code	MBL
Device class	Class II
Decision date	Oct 22, 2012
Decision	Substantially Equivalent
Regulation	888.3358

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Source

View the full FDA submission: accessdata.fda.gov

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DYNASTY BIOFOAM SHELL

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