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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 a medical device manufactured by Trident Orthopedics. It received FDA 510(k) clearance on 2018-05-08 under approval 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. It is manufactured by Trident Orthopedics. The 510(k) number is K171690.

When was Trident Extremity Fixation System approved by the FDA?

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

What company makes Trident Extremity Fixation System?

Trident Extremity Fixation System is manufactured by Trident Orthopedics.

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

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

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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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