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FDA 510(k)

RIBBOND - TRIAXIAL

K-Number: K013881 · 2002-01-25

ApplicantRibbond, Inc.
Decision Date2002-01-25
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RIBBOND - TRIAXIAL is the device name listed in this FDA 510(k) record. The listed applicant is Ribbond, Inc.. It received FDA 510(k) clearance on 2002-01-25 under 510(k) number K013881. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIBBOND - TRIAXIAL?

RIBBOND - TRIAXIAL is a medical device that received FDA 510(k) clearance on 2002-01-25. The listed applicant is Ribbond, Inc.. The 510(k) number is K013881.

When did RIBBOND - TRIAXIAL receive FDA 510(k) clearance?

RIBBOND - TRIAXIAL received FDA 510(k) clearance on 2002-01-25, under 510(k) number K013881.

Who is the listed applicant for RIBBOND - TRIAXIAL?

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

What is the FDA product code for RIBBOND - TRIAXIAL?

The FDA product code for RIBBOND - TRIAXIAL is EBI.

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Other records listing Ribbond, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K913040RIBBOND(TM)

Related Devices (Code: EBI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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