NuVasive AttraX Putty
K-Number: K191974 · 2019-11-03
ApplicantNu Vasive, Incorporated
Decision Date2019-11-03
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
NuVasive AttraX Putty is a medical device manufactured by Nu Vasive, Incorporated. It received FDA 510(k) clearance on 2019-11-03 under approval number K191974. 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 Putty?
NuVasive AttraX Putty is a medical device that received FDA 510(k) clearance on 2019-11-03. It is manufactured by Nu Vasive, Incorporated. The 510(k) number is K191974.
When was NuVasive AttraX Putty approved by the FDA?
NuVasive AttraX Putty received FDA 510(k) clearance on 2019-11-03, under approval number K191974.
What company makes NuVasive AttraX Putty?
NuVasive AttraX Putty is manufactured by Nu Vasive, Incorporated.
What is the FDA product code for NuVasive AttraX Putty?
The FDA product code for NuVasive AttraX Putty 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.