K-number	K123352
Device name	S4 SPINAL SYSTEM
Applicant	Aesculap Implant Systems, Inc.
Product code	NKB
Device class	Class II
Decision date	Dec 12, 2012
Decision	Substantially Equivalent
Regulation	888.3070

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Source

View the full FDA submission: accessdata.fda.gov

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S4 SPINAL SYSTEM

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