K-number	K914715
Device name	PARALLELING GUIDES
Applicant	Implant Corp. of America
Product code	FZX
Device class	Class I
Decision date	Feb 16, 1994
Decision	Substantially Equivalent
Regulation	878.4800

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View the full FDA submission: accessdata.fda.gov

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PARALLELING GUIDES

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