NuVasive ACP System
K-Number: K203253 · 2020-12-03
ApplicantNu Vasive, Incorporated
Decision Date2020-12-03
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
NuVasive ACP System is a medical device manufactured by Nu Vasive, Incorporated. It received FDA 510(k) clearance on 2020-12-03 under approval number K203253. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the NuVasive ACP System?
NuVasive ACP System is a medical device that received FDA 510(k) clearance on 2020-12-03. It is manufactured by Nu Vasive, Incorporated. The 510(k) number is K203253.
When was NuVasive ACP System approved by the FDA?
NuVasive ACP System received FDA 510(k) clearance on 2020-12-03, under approval number K203253.
What company makes NuVasive ACP System?
NuVasive ACP System is manufactured by Nu Vasive, Incorporated.
What is the FDA product code for NuVasive ACP System?
The FDA product code for NuVasive ACP System is KWQ.
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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.