TriMed Bridge Plates
K-Number: K241942 · 2024-09-17
ApplicantTriMed, Inc.
Decision Date2024-09-17
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
TriMed Bridge Plates is a medical device manufactured by TriMed, Inc.. It received FDA 510(k) clearance on 2024-09-17 under approval number K241942. 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 Bridge Plates?
TriMed Bridge Plates is a medical device that received FDA 510(k) clearance on 2024-09-17. It is manufactured by TriMed, Inc.. The 510(k) number is K241942.
When was TriMed Bridge Plates approved by the FDA?
TriMed Bridge Plates received FDA 510(k) clearance on 2024-09-17, under approval number K241942.
What company makes TriMed Bridge Plates?
TriMed Bridge Plates is manufactured by TriMed, Inc..
What is the FDA product code for TriMed Bridge Plates?
The FDA product code for TriMed Bridge Plates 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.