K-number	K800363
Device name	PARKE-DAVIS TOTAL KNEE PROSTHESIS
Applicant	Warner-Lambert Co.
Product code	KTZ
Device class	Class I
Decision date	Mar 10, 1980
Decision	Substantially Equivalent
Regulation	888.4150

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View the full FDA submission: accessdata.fda.gov

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PARKE-DAVIS TOTAL KNEE PROSTHESIS

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