K-number	K803031
Device name	LAURE WRIST IMPLANT
Applicant	Laure Prosthetics, Inc.
Product code	KWM
Device class	Class II
Decision date	Jun 29, 1982
Decision	Substantially Equivalent
Regulation	888.3800

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View the full FDA submission: accessdata.fda.gov

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LAURE WRIST IMPLANT

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