NuVasive 3DP Interfixated ALIF System
K-Number: K193593 · 2020-03-25
ApplicantNu Vasive, Incorporated
Decision Date2020-03-25
Product CodeOVD
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
NuVasive 3DP Interfixated ALIF System is a medical device manufactured by Nu Vasive, Incorporated. It received FDA 510(k) clearance on 2020-03-25 under approval number K193593. The device is classified under product code OVD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the NuVasive 3DP Interfixated ALIF System?
NuVasive 3DP Interfixated ALIF System is a medical device that received FDA 510(k) clearance on 2020-03-25. It is manufactured by Nu Vasive, Incorporated. The 510(k) number is K193593.
When was NuVasive 3DP Interfixated ALIF System approved by the FDA?
NuVasive 3DP Interfixated ALIF System received FDA 510(k) clearance on 2020-03-25, under approval number K193593.
What company makes NuVasive 3DP Interfixated ALIF System?
NuVasive 3DP Interfixated ALIF System is manufactured by Nu Vasive, Incorporated.
What is the FDA product code for NuVasive 3DP Interfixated ALIF System?
The FDA product code for NuVasive 3DP Interfixated ALIF System is OVD.
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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.