K-number	K925351
Device name	SYNTHES(U.S.A.) ANTERIOR SPINAL PLATE
Applicant	Synthes (Usa)
Product code	KWQ
Device class	Class II
Decision date	Nov 5, 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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SYNTHES(U.S.A.) ANTERIOR SPINAL PLATE

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