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 a medical device manufactured by TriMed, Inc.. It received FDA 510(k) clearance on 2022-12-21 under approval 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. It is manufactured by TriMed, Inc.. The 510(k) number is K222637.
When was TriMed Wrist Fixation System 3 approved by the FDA?
TriMed Wrist Fixation System 3 received FDA 510(k) clearance on 2022-12-21, under approval number K222637.
What company makes TriMed Wrist Fixation System 3?
TriMed Wrist Fixation System 3 is manufactured by TriMed, Inc..
What is the FDA product code for TriMed Wrist Fixation System 3?
The FDA product code for TriMed Wrist Fixation System 3 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.