K-number	K080426
Device name	MAESTRO WRIST FRACTURE IMPLANT
Applicant	Biomet Manufacturing Corp
Product code	JWJ
Device class	Class II
Decision date	Jul 29, 2008
Decision	Substantially Equivalent
Regulation	888.3800

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Source

View the full FDA submission: accessdata.fda.gov

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MAESTRO WRIST FRACTURE IMPLANT

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