NuVasiveNVM5 System
K-Number: K152942 · 2016-01-13
ApplicantNu Vasive, Incorporated
Decision Date2016-01-13
Product CodePDQ
Advisory CommitteeEN
DecisionSubstantially Equivalent
Device Summary
NuVasiveNVM5 System is a medical device manufactured by Nu Vasive, Incorporated. It received FDA 510(k) clearance on 2016-01-13 under approval number K152942. The device is classified under product code PDQ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the NuVasiveNVM5 System?
NuVasiveNVM5 System is a medical device that received FDA 510(k) clearance on 2016-01-13. It is manufactured by Nu Vasive, Incorporated. The 510(k) number is K152942.
When was NuVasiveNVM5 System approved by the FDA?
NuVasiveNVM5 System received FDA 510(k) clearance on 2016-01-13, under approval number K152942.
What company makes NuVasiveNVM5 System?
NuVasiveNVM5 System is manufactured by Nu Vasive, Incorporated.
What is the FDA product code for NuVasiveNVM5 System?
The FDA product code for NuVasiveNVM5 System is PDQ.
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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.