K-number	K113802
Device name	ESCALATE LAMINOPLASTY SYSTEM
Applicant	Stryker Spine
Product code	NQW
Device class	Class II
Decision date	Apr 16, 2012
Decision	Substantially Equivalent
Regulation	888.3050

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Source

View the full FDA submission: accessdata.fda.gov

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ESCALATE LAMINOPLASTY SYSTEM

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