FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Distal Xtremities System

K Number: K252061 · Decision Aug 20, 2025
Classifications
1
FEI Numbers
519
Registration Numbers
519
Same Product Code
1313
Applicant Total
36
Review Days
50

Basic Information

Device Name
Distal Xtremities System
K Number
K252061
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
TriMed, Inc.
Date Received
July 1, 2025
Decision Date
August 20, 2025
Product Code
HRS
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HRS Plate, Fixation, Bone

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Other Clearances by TriMed, Inc.

K Number Device Name
K261241 TriMed Compression Screws
K254002 TriMed Volar Bearing Plates (VBEAL-13-7S); TriMed Volar Bearing Plates (VBEAR-13-7S); TriMed Volar Bearing Plates (VBEAL-14-7S); TriMed Volar Bearing Plates (VBEAR-14-7S); TriMed Volar Bearing Plates (VBEAL-16-7S); TriMed Volar Bearing Plates (VBEAR-16-7S)
K251134 RipCord
K251945 TriMed Total Wrist Fusion System (Total Wrist Fusion Plate)
K250929 TriMed Ulnar Osteotomy System (Ulnar Osteotomy Compression Plate); TriMed Ulnar Osteotomy System (Hex Cortical Screw 3.2mm); TriMed Ulnar Osteotomy System (Locking Cortical Screw 3.2mm); TriMed Ulnar Osteotomy System (Lag Screw 3.2mm)
K250935 TriMed Fifth Metatarsal System (Fifth Metatarsal Plate); TriMed Fifth Metatarsal System (Fifth Metatarsal Screw)
K243943 TriMed® Compression Screws
K250948 TriMed Fusion Cup System
K243987 TriMed Elbow and Forearm System
K243999 TriMed Ankle Fixation System
Search all 36 clearances from TriMed, Inc. →