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FDA 510(k)

Bendini Cloud Application

K-Number: K233706 · 2024-08-02

ApplicantNuvasive
Decision Date2024-08-02
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Bendini Cloud Application is the device name listed in this FDA 510(k) record. The listed applicant is Nuvasive. It received FDA 510(k) clearance on 2024-08-02 under 510(k) number K233706. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Bendini Cloud Application?

Bendini Cloud Application is a medical device that received FDA 510(k) clearance on 2024-08-02. The listed applicant is Nuvasive. The 510(k) number is K233706.

When did Bendini Cloud Application receive FDA 510(k) clearance?

Bendini Cloud Application received FDA 510(k) clearance on 2024-08-02, under 510(k) number K233706.

Who is the listed applicant for Bendini Cloud Application?

The FDA 510(k) record lists Nuvasive as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Bendini Cloud Application?

The FDA product code for Bendini Cloud Application is OLO.

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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.

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