NuVasive AttraX Scaffold
K-Number: K172497 · 2017-11-24
ApplicantNu Vasive, Incorporated
Decision Date2017-11-24
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
NuVasive AttraX Scaffold is a medical device manufactured by Nu Vasive, Incorporated. It received FDA 510(k) clearance on 2017-11-24 under approval number K172497. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the NuVasive AttraX Scaffold?
NuVasive AttraX Scaffold is a medical device that received FDA 510(k) clearance on 2017-11-24. It is manufactured by Nu Vasive, Incorporated. The 510(k) number is K172497.
When was NuVasive AttraX Scaffold approved by the FDA?
NuVasive AttraX Scaffold received FDA 510(k) clearance on 2017-11-24, under approval number K172497.
What company makes NuVasive AttraX Scaffold?
NuVasive AttraX Scaffold is manufactured by Nu Vasive, Incorporated.
What is the FDA product code for NuVasive AttraX Scaffold?
The FDA product code for NuVasive AttraX Scaffold is MQV.
Other Devices by Nu Vasive, Incorporated
Related Devices (Code: MQV)
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.