NuVasive® CoRoent® Small Interlock System
K-Number: K161442 · 2016-09-28
ApplicantNu Vasive, Incorporated
Decision Date2016-09-28
Product CodeOVE
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
NuVasive® CoRoent® Small Interlock System is a medical device manufactured by Nu Vasive, Incorporated. It received FDA 510(k) clearance on 2016-09-28 under approval number K161442. The device is classified under product code OVE. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the NuVasive® CoRoent® Small Interlock System?
NuVasive® CoRoent® Small Interlock System is a medical device that received FDA 510(k) clearance on 2016-09-28. It is manufactured by Nu Vasive, Incorporated. The 510(k) number is K161442.
When was NuVasive® CoRoent® Small Interlock System approved by the FDA?
NuVasive® CoRoent® Small Interlock System received FDA 510(k) clearance on 2016-09-28, under approval number K161442.
What company makes NuVasive® CoRoent® Small Interlock System?
NuVasive® CoRoent® Small Interlock System is manufactured by Nu Vasive, Incorporated.
What is the FDA product code for NuVasive® CoRoent® Small Interlock System?
The FDA product code for NuVasive® CoRoent® Small Interlock System is OVE.
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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.