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

Arthrex Anatomic Lapidus Plates and I-Beam Lapidus Plates

K Number: K252807 · Decision Jan 12, 2026
Classifications
1
FEI Numbers
519
Registration Numbers
519
Same Product Code
1313
Applicant Total
348
Review Days
131

Basic Information

Device Name
Arthrex Anatomic Lapidus Plates and I-Beam Lapidus Plates
K Number
K252807
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Arthrex, Inc.
Date Received
September 3, 2025
Decision Date
January 12, 2026
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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