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FDA 510(k)

Rebuilder Nerve Guidance Conduit

K-Number: K230794 · 2024-01-29

ApplicantCelestray Biotech Company, LLC.,
Decision Date2024-01-29
Product CodeJXI
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Rebuilder Nerve Guidance Conduit is a medical device manufactured by Celestray Biotech Company, LLC.,. It received FDA 510(k) clearance on 2024-01-29 under approval number K230794. The device is classified under product code JXI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Rebuilder Nerve Guidance Conduit?

Rebuilder Nerve Guidance Conduit is a medical device that received FDA 510(k) clearance on 2024-01-29. It is manufactured by Celestray Biotech Company, LLC.,. The 510(k) number is K230794.

When was Rebuilder Nerve Guidance Conduit approved by the FDA?

Rebuilder Nerve Guidance Conduit received FDA 510(k) clearance on 2024-01-29, under approval number K230794.

What company makes Rebuilder Nerve Guidance Conduit?

Rebuilder Nerve Guidance Conduit is manufactured by Celestray Biotech Company, LLC.,.

What is the FDA product code for Rebuilder Nerve Guidance Conduit?

The FDA product code for Rebuilder Nerve Guidance Conduit is JXI.

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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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