STRYKER NAVIGATION SYSTEM - NEURO MODULE, MODEL 6000-XXX-XXX (K993239) — FDA 510(k) Clearance | Predicase

K-number	K993239
Device name	STRYKER NAVIGATION SYSTEM - NEURO MODULE, MODEL 6000-XXX-XXX
Applicant	Stryker Corp.
Product code	HAW
Device class	Class II
Decision date	Jan 18, 2000
Decision	Substantially Equivalent
Regulation	882.4560

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Source

View the full FDA submission: accessdata.fda.gov

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