K-number	K032527
Device name	HEDROCEL VERTEBRAL BODY REPLACEMENT
Applicant	Implex Corp.
Product code	MQP
Device class	Class II
Decision date	Oct 31, 2003
Decision	Substantially Equivalent
Regulation	888.3060

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View the full FDA submission: accessdata.fda.gov

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HEDROCEL VERTEBRAL BODY REPLACEMENT

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