K-number	K030039
Device name	PATHWAY STM-10 PELVIC FLOOR STIMULATOR
Applicant	The Prometheus Group
Product code	KPI
Device class	Class II
Decision date	May 23, 2003
Decision	Substantially Equivalent
Regulation	876.5320

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Source

View the full FDA submission: accessdata.fda.gov

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PATHWAY STM-10 PELVIC FLOOR STIMULATOR

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