K-number	K032601
Device name	STRYKER INTERVENTIONAL PAIN RF GENERATOR
Applicant	Valley Forge Scientific Corp.
Product code	GXD
Device class	Class II
Decision date	Apr 1, 2004
Decision	Substantially Equivalent
Regulation	882.4400

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View the full FDA submission: accessdata.fda.gov

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STRYKER INTERVENTIONAL PAIN RF GENERATOR

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