K-number	K040417
Device name	PILLAR PALATAL IMPLANT SYSTEM
Applicant	Restore Medical, Inc.
Product code	LRK
Device class	Class II
Decision date	Jul 28, 2004
Decision	Substantially Equivalent
Regulation	872.5570

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View the full FDA submission: accessdata.fda.gov

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PILLAR PALATAL IMPLANT SYSTEM

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