K-number	K053276
Device name	IST PEDICLE SCREW SYSTEM
Applicant	Innovative Spinal Technologies, Inc.
Product code	NKB
Device class	Class II
Decision date	Dec 27, 2005
Decision	Substantially Equivalent
Regulation	888.3070

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View the full FDA submission: accessdata.fda.gov

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IST PEDICLE SCREW SYSTEM

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