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FDA 510(k)

Trivergent Spinal Fixation System

K-Number: K201427 · 2020-10-21

Decision Date2020-10-21
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Trivergent Spinal Fixation System is the device name listed in this FDA 510(k) record. The listed applicant is Benvenue Medical, Inc.. It received FDA 510(k) clearance on 2020-10-21 under 510(k) number K201427. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Trivergent Spinal Fixation System?

Trivergent Spinal Fixation System is a medical device that received FDA 510(k) clearance on 2020-10-21. The listed applicant is Benvenue Medical, Inc.. The 510(k) number is K201427.

When did Trivergent Spinal Fixation System receive FDA 510(k) clearance?

Trivergent Spinal Fixation System received FDA 510(k) clearance on 2020-10-21, under 510(k) number K201427.

Who is the listed applicant for Trivergent Spinal Fixation System?

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

What is the FDA product code for Trivergent Spinal Fixation System?

The FDA product code for Trivergent Spinal Fixation System is NKB.

Other records listing Benvenue Medical, 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.

Related Devices (Code: NKB)

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.

Official Source

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