FDA 510(k)

Rod Registration Frame

K-Number: K230989 · 2023-05-05

Decision Date2023-05-05

Product CodeOLO

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

Rod Registration Frame is a medical device manufactured by Nu Vasive, Incorporated. It received FDA 510(k) clearance on 2023-05-05 under approval number K230989. 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 Rod Registration Frame?

Rod Registration Frame is a medical device that received FDA 510(k) clearance on 2023-05-05. It is manufactured by Nu Vasive, Incorporated. The 510(k) number is K230989.

When was Rod Registration Frame approved by the FDA?

Rod Registration Frame received FDA 510(k) clearance on 2023-05-05, under approval number K230989.

What company makes Rod Registration Frame?

Rod Registration Frame is manufactured by Nu Vasive, Incorporated.

What is the FDA product code for Rod Registration Frame?

The FDA product code for Rod Registration Frame is OLO.

Other Devices by Nu Vasive, Incorporated

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Related Devices (Code: 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.