NuVasive Reline System
K-Number: K223181 · 2023-01-11
ApplicantNu Vasive, Incorporated
Decision Date2023-01-11
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
NuVasive Reline System is a medical device manufactured by Nu Vasive, Incorporated. It received FDA 510(k) clearance on 2023-01-11 under approval number K223181. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the NuVasive Reline System?
NuVasive Reline System is a medical device that received FDA 510(k) clearance on 2023-01-11. It is manufactured by Nu Vasive, Incorporated. The 510(k) number is K223181.
When was NuVasive Reline System approved by the FDA?
NuVasive Reline System received FDA 510(k) clearance on 2023-01-11, under approval number K223181.
What company makes NuVasive Reline System?
NuVasive Reline System is manufactured by Nu Vasive, Incorporated.
What is the FDA product code for NuVasive Reline System?
The FDA product code for NuVasive Reline System is NKB.
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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.