K-number	K090767
Device name	PERPOS FCD-2 SYSTEM (SINGLE PATIENT USE), ANCHOR, STABILIZER
Applicant	Interventional Spine, Inc.
Product code	MRW
Device class	Class U
Decision date	Jun 11, 2009
Decision	Unknown
Regulation	—

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PERPOS FCD-2 SYSTEM (SINGLE PATIENT USE), ANCHOR, STABILIZER

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