K-number	K820047
Device name	SPINOCAN SPINAL NEEDLE
Applicant	Burron Medical Products, Inc.
Product code	BSP
Device class	Class II
Decision date	Jan 25, 1982
Decision	Substantially Equivalent
Regulation	868.5150

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View the full FDA submission: accessdata.fda.gov

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SPINOCAN SPINAL NEEDLE

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