K-number	K051879
Device name	SYNTHES (USA) POROUS POLYETHYLENE IMPLANTS
Applicant	Synthes (Usa)
Product code	FTM
Device class	Class II
Decision date	Oct 5, 2005
Decision	Substantially Equivalent
Regulation	878.3300

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View the full FDA submission: accessdata.fda.gov

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SYNTHES (USA) POROUS POLYETHYLENE IMPLANTS

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