K-number	K970285
Device name	AESUCLAP SOCON SPINAL SYSTEM
Applicant	Aesculap, Inc.
Product code	MNH
Device class	Class II
Decision date	Jun 25, 1997
Decision	Substantially Equivalent
Regulation	888.3070

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View the full FDA submission: accessdata.fda.gov

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AESUCLAP SOCON SPINAL SYSTEM

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