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FDA 510(k)

TriMed ASET Foot Plating System

K-Number: K192696 · 2020-01-05

ApplicantTriMed, Inc.
Decision Date2020-01-05
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TriMed ASET Foot Plating System is a medical device manufactured by TriMed, Inc.. It received FDA 510(k) clearance on 2020-01-05 under approval number K192696. 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 ASET Foot Plating System?

TriMed ASET Foot Plating System is a medical device that received FDA 510(k) clearance on 2020-01-05. It is manufactured by TriMed, Inc.. The 510(k) number is K192696.

When was TriMed ASET Foot Plating System approved by the FDA?

TriMed ASET Foot Plating System received FDA 510(k) clearance on 2020-01-05, under approval number K192696.

What company makes TriMed ASET Foot Plating System?

TriMed ASET Foot Plating System is manufactured by TriMed, Inc..

What is the FDA product code for TriMed ASET Foot Plating System?

The FDA product code for TriMed ASET Foot Plating System is HRS.

Other Devices by TriMed, Inc.

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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.