K-number	K923703
Device name	KANEDA ANTERIOR SPINAL MULTISEGMENTAL FIXATION DEV
Applicant	Acromed Corp.
Product code	KWQ
Device class	Class II
Decision date	May 20, 1993
Decision	Substantially Equivalent for Some Indications
Regulation	888.3060

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View the full FDA submission: accessdata.fda.gov

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KANEDA ANTERIOR SPINAL MULTISEGMENTAL FIXATION DEV

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