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FDA 510(k)

Trident Extremity Fixation System

K-Number: K171690 · 2018-05-08

ApplicantTrident Orthopedics
Decision Date2018-05-08
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Trident Extremity Fixation System is the device name listed in this FDA 510(k) record. The listed applicant is Trident Orthopedics. It received FDA 510(k) clearance on 2018-05-08 under 510(k) number K171690. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Trident Extremity Fixation System?

Trident Extremity Fixation System is a medical device that received FDA 510(k) clearance on 2018-05-08. The listed applicant is Trident Orthopedics. The 510(k) number is K171690.

When did Trident Extremity Fixation System receive FDA 510(k) clearance?

Trident Extremity Fixation System received FDA 510(k) clearance on 2018-05-08, under 510(k) number K171690.

Who is the listed applicant for Trident Extremity Fixation System?

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

What is the FDA product code for Trident Extremity Fixation System?

The FDA product code for Trident Extremity Fixation System is HRS.

Related Devices (Code: HRS)

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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