K-number	K111122
Device name	AESCULAP SIBD XP SPINAL SYSTEM
Applicant	Aesculap Implant Systems, Inc.
Product code	OVD
Device class	Class II
Decision date	Aug 4, 2011
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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AESCULAP SIBD XP SPINAL SYSTEM

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