K-number	K982368
Device name	MANIFOLD WITH EXTENSION SET
Applicant	Interpore Cross Intl.
Product code	FMG
Device class	Class II
Decision date	Jul 31, 1998
Decision	Substantially Equivalent
Regulation	880.5440

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View the full FDA submission: accessdata.fda.gov

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MANIFOLD WITH EXTENSION SET

Everything you need for a 510(k) submission. Nothing you don't.