K-number	K781091
Device name	KNEE INSTRUMENTATION, CONDYLAR
Applicant	Biomet, Inc.
Product code	HWT
Device class	Class I
Decision date	Jul 17, 1978
Decision	Substantially Equivalent
Regulation	888.4800

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View the full FDA submission: accessdata.fda.gov

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KNEE INSTRUMENTATION, CONDYLAR

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