K-number	K160222
Device name	OIC Cervical PEEK Spacer
Applicant	The Orthopaedic Implant Company
Product code	ODP
Device class	Class II
Decision date	Dec 7, 2016
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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OIC Cervical PEEK Spacer

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