K-number	K083311
Device name	AESCULAP CESPACE PEEK INTERVERTEBRAL BODY FUSION SYSTEM
Applicant	Aesculap Implant Systems, Inc.
Product code	ODP
Device class	Class II
Decision date	Mar 4, 2009
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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AESCULAP CESPACE PEEK INTERVERTEBRAL BODY FUSION SYSTEM

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