K-number	K022644
Device name	RETRO REPAIR KIT, MODEL PRRK5
Applicant	Spire Biomedical, Inc.
Product code	NFK
Device class	Class II
Decision date	Nov 6, 2002
Decision	Unknown
Regulation	876.5540

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View the full FDA submission: accessdata.fda.gov

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RETRO REPAIR KIT, MODEL PRRK5

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