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FDA 510(k)

TriMed Wrist Fixation System 3

K-Number: K222637 · 2022-12-21

ApplicantTriMed, Inc.
Decision Date2022-12-21
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TriMed Wrist Fixation System 3 is the device name listed in this FDA 510(k) record. The listed applicant is TriMed, Inc.. It received FDA 510(k) clearance on 2022-12-21 under 510(k) number K222637. 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 Wrist Fixation System 3?

TriMed Wrist Fixation System 3 is a medical device that received FDA 510(k) clearance on 2022-12-21. The listed applicant is TriMed, Inc.. The 510(k) number is K222637.

When did TriMed Wrist Fixation System 3 receive FDA 510(k) clearance?

TriMed Wrist Fixation System 3 received FDA 510(k) clearance on 2022-12-21, under 510(k) number K222637.

Who is the listed applicant for TriMed Wrist Fixation System 3?

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

What is the FDA product code for TriMed Wrist Fixation System 3?

The FDA product code for TriMed Wrist Fixation System 3 is HRS.

Other records listing TriMed, 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.

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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.

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.