K-number	K980121
Device name	AESCULAP SPINE SYSTEM ADDITIONAL COMPONENTS
Applicant	Aesculap, Inc.
Product code	KWP
Device class	Class II
Decision date	Jun 10, 1998
Decision	Substantially Equivalent
Regulation	888.3050

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View the full FDA submission: accessdata.fda.gov

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AESCULAP SPINE SYSTEM ADDITIONAL COMPONENTS

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