K-number	K940207
Device name	TITANIUM ALLOY BONE SCREWS
Applicant	Aesculap, Inc.
Product code	HWC
Device class	Class II
Decision date	Jul 12, 1994
Decision	Substantially Equivalent
Regulation	888.3040

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View the full FDA submission: accessdata.fda.gov

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TITANIUM ALLOY BONE SCREWS

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