NuVasive CoRoent Small Interbody System
K-Number: K163491 · 2017-03-24
ApplicantNu Vasive, Incorporated
Decision Date2017-03-24
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
NuVasive CoRoent Small Interbody System is a medical device manufactured by Nu Vasive, Incorporated. It received FDA 510(k) clearance on 2017-03-24 under approval number K163491. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the NuVasive CoRoent Small Interbody System?
NuVasive CoRoent Small Interbody System is a medical device that received FDA 510(k) clearance on 2017-03-24. It is manufactured by Nu Vasive, Incorporated. The 510(k) number is K163491.
When was NuVasive CoRoent Small Interbody System approved by the FDA?
NuVasive CoRoent Small Interbody System received FDA 510(k) clearance on 2017-03-24, under approval number K163491.
What company makes NuVasive CoRoent Small Interbody System?
NuVasive CoRoent Small Interbody System is manufactured by Nu Vasive, Incorporated.
What is the FDA product code for NuVasive CoRoent Small Interbody System?
The FDA product code for NuVasive CoRoent Small Interbody System is ODP.
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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.