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FDA 510(k)

NerveTape

K-Number: K233533 · 2024-02-12

ApplicantBiocircuit Technologies, Inc.
Decision Date2024-02-12
Product CodeJXI
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NerveTape is a medical device manufactured by Biocircuit Technologies, Inc.. It received FDA 510(k) clearance on 2024-02-12 under approval number K233533. 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 NerveTape?

NerveTape is a medical device that received FDA 510(k) clearance on 2024-02-12. It is manufactured by Biocircuit Technologies, Inc.. The 510(k) number is K233533.

When was NerveTape approved by the FDA?

NerveTape received FDA 510(k) clearance on 2024-02-12, under approval number K233533.

What company makes NerveTape?

NerveTape is manufactured by Biocircuit Technologies, Inc..

What is the FDA product code for NerveTape?

The FDA product code for NerveTape is JXI.

Other Devices by Biocircuit Technologies, Inc.

K242113Nerve Wrap (07-DW-001-TAB)

Related Devices (Code: JXI)

K162741AxoGuard Nerve ConnectorCook Biotech Incorporated K152967NERBRIDGEToyobo Co., Ltd. K152684Nerve Capping DevicePolyganics Innovations BV K163446AxoGen Nerve CapAxogen Corporation K170656Reinforced Flexible Collagen Nerve CuffCollagen Matrix, Inc. K163457NeuraGen 3D Nerve Guide MatrixIntegra LifeSciences Corporation

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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