K-number	K781870
Device name	IMPLANT, H.P. CONDYLAR
Applicant	Dow Corning Corp. Healthcare Industries Materials
Product code	KWD
Device class	Class II
Decision date	Feb 9, 1979
Decision	Substantially Equivalent
Regulation	888.3730

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View the full FDA submission: accessdata.fda.gov

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IMPLANT, H.P. CONDYLAR

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