NuVasive® Precept Spinal System
K-Number: K171894 · 2017-09-28
ApplicantNu Vasive, Incorporated
Decision Date2017-09-28
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
NuVasive® Precept Spinal System is a medical device manufactured by Nu Vasive, Incorporated. It received FDA 510(k) clearance on 2017-09-28 under approval number K171894. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the NuVasive® Precept Spinal System?
NuVasive® Precept Spinal System is a medical device that received FDA 510(k) clearance on 2017-09-28. It is manufactured by Nu Vasive, Incorporated. The 510(k) number is K171894.
When was NuVasive® Precept Spinal System approved by the FDA?
NuVasive® Precept Spinal System received FDA 510(k) clearance on 2017-09-28, under approval number K171894.
What company makes NuVasive® Precept Spinal System?
NuVasive® Precept Spinal System is manufactured by Nu Vasive, Incorporated.
What is the FDA product code for NuVasive® Precept Spinal System?
The FDA product code for NuVasive® Precept Spinal System is NKB.
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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.