K-number	K990059
Device name	OSTEONICS SPINAL SYSTEM-EXPANDED INDICATIONS
Applicant	Howmedica Osteonics Corp.
Product code	MNI
Device class	Class II
Decision date	Jan 28, 1999
Decision	Substantially Equivalent
Regulation	888.3070

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View the full FDA submission: accessdata.fda.gov

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OSTEONICS SPINAL SYSTEM-EXPANDED INDICATIONS

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