NuVasive CoRoent Ti-C System
K-Number: K163707 · 2017-05-01
ApplicantNu Vasive, Incorporated
Decision Date2017-05-01
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
NuVasive CoRoent Ti-C System is a medical device manufactured by Nu Vasive, Incorporated. It received FDA 510(k) clearance on 2017-05-01 under approval number K163707. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the NuVasive CoRoent Ti-C System?
NuVasive CoRoent Ti-C System is a medical device that received FDA 510(k) clearance on 2017-05-01. It is manufactured by Nu Vasive, Incorporated. The 510(k) number is K163707.
When was NuVasive CoRoent Ti-C System approved by the FDA?
NuVasive CoRoent Ti-C System received FDA 510(k) clearance on 2017-05-01, under approval number K163707.
What company makes NuVasive CoRoent Ti-C System?
NuVasive CoRoent Ti-C System is manufactured by Nu Vasive, Incorporated.
What is the FDA product code for NuVasive CoRoent Ti-C System?
The FDA product code for NuVasive CoRoent Ti-C System is MAX.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.