K-number	K033930
Device name	KAPP CUSTOM ULNAR HEAD WRIST IMPLANT
Applicant	Kapp Surgical Instrument, Inc.
Product code	KXE
Device class	Class II
Decision date	Jul 28, 2004
Decision	Substantially Equivalent
Regulation	888.3810

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View the full FDA submission: accessdata.fda.gov

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KAPP CUSTOM ULNAR HEAD WRIST IMPLANT

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