K-number	K850024
Device name	ORTHOPEDIC IMPLANT SCREWS
Applicant	Kirkstil Corp., Inc.
Product code	HWC
Device class	Class II
Decision date	May 20, 1985
Decision	Substantially Equivalent
Regulation	888.3040

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View the full FDA submission: accessdata.fda.gov

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ORTHOPEDIC IMPLANT SCREWS

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