K-number	K132122
Device name	KESTREL POSTERIOR CERVICAL SPINE SYSTEM
Applicant	Omni Surgical, LLC Dba Spine360
Product code	KWP
Device class	Class II
Decision date	Jan 22, 2014
Decision	Substantially Equivalent
Regulation	888.3050

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Source

View the full FDA submission: accessdata.fda.gov

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KESTREL POSTERIOR CERVICAL SPINE SYSTEM

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