K-number	K103205
Device name	BRIDGEPOINT SPINOUS PROCESS CAMP- POSTERIOR FIXATION SYSTEM
Applicant	Alphatec Spine, Inc.
Product code	KWP
Device class	Class II
Decision date	Jun 2, 2011
Decision	Substantially Equivalent
Regulation	888.3050

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View the full FDA submission: accessdata.fda.gov

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BRIDGEPOINT SPINOUS PROCESS CAMP- POSTERIOR FIXATION SYSTEM

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