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FDA 510(k)

TriMed Clavicle Fixation System

K-Number: K230805 · 2023-09-01

ApplicantTriMed, Inc.
Decision Date2023-09-01
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TriMed Clavicle Fixation System is a medical device manufactured by TriMed, Inc.. It received FDA 510(k) clearance on 2023-09-01 under approval number K230805. 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 TriMed Clavicle Fixation System?

TriMed Clavicle Fixation System is a medical device that received FDA 510(k) clearance on 2023-09-01. It is manufactured by TriMed, Inc.. The 510(k) number is K230805.

When was TriMed Clavicle Fixation System approved by the FDA?

TriMed Clavicle Fixation System received FDA 510(k) clearance on 2023-09-01, under approval number K230805.

What company makes TriMed Clavicle Fixation System?

TriMed Clavicle Fixation System is manufactured by TriMed, Inc..

What is the FDA product code for TriMed Clavicle Fixation System?

The FDA product code for TriMed Clavicle Fixation System is HRS.

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Other Devices by TriMed, Inc.

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Related Devices (Code: 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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