K-number	K972718
Device name	M-2 ANTERIOR PLATE SYSTEM
Applicant	Acromed Corp.
Product code	KWQ
Device class	Class II
Decision date	Oct 1, 1997
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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M-2 ANTERIOR PLATE SYSTEM

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