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

OrthoPediatrics® Locking Cannulated Blade Plate System

K Number: K260323 · Decision Apr 30, 2026
Classifications
1
FEI Numbers
519
Registration Numbers
519
Same Product Code
1313
Applicant Total
40
Review Days
90

Basic Information

Device Name
OrthoPediatrics® Locking Cannulated Blade Plate System
K Number
K260323
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
OrthoPediatrics Corp.
Date Received
January 30, 2026
Decision Date
April 30, 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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