K-number	K992782
Device name	NUVASIVE SPINAL ARTHROSCOPE, MODELS 0, 30 AND 70 DEGREES
Applicant	Nuvasive, Inc.
Product code	HRX
Device class	Class II
Decision date	Oct 5, 1999
Decision	Substantially Equivalent
Regulation	888.1100

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View the full FDA submission: accessdata.fda.gov

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NUVASIVE SPINAL ARTHROSCOPE, MODELS 0, 30 AND 70 DEGREES

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