K-number	K192396
Device name	Streamline MIS Spinal Fixation System
Applicant	Pioneer Surgical Technology, Inc.
Product code	NKB
Device class	Class II
Decision date	Nov 26, 2019
Decision	Substantially Equivalent
Regulation	888.3070

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Source

View the full FDA submission: accessdata.fda.gov

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Streamline MIS Spinal Fixation System

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