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

ATLAS™ Expandable Osteotomy Wedge System

K Number: K252733 · Decision Feb 19, 2026
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
17
Applicant Total
24
Review Days
175

Basic Information

Device Name
ATLAS™ Expandable Osteotomy Wedge System
K Number
K252733
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MiRus, LLC
Date Received
August 28, 2025
Decision Date
February 19, 2026
Product Code
PLF
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
PLF Bone Wedge

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