FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

Fitbone™ Trochanteric, FITBONE® Transport and Lengthening System, FITBONE® TAA

K Number: K253991 · Decision May 8, 2026
Classifications
1
FEI Numbers
302
Registration Numbers
302
Same Product Code
528
Applicant Total
38
Review Days
147

Basic Information

Device Name
Fitbone™ Trochanteric, FITBONE® Transport and Lengthening System, FITBONE® TAA
K Number
K253991
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3020
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Orthofix Srl
Date Received
December 12, 2025
Decision Date
May 8, 2026
Product Code
HSB
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
HSB Rod, Fixation, Intramedullary And Accessories

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Other Clearances by Orthofix Srl

K Number Device Name
K260146 FITBONE® TRANSPORT AND LENGTHENING SYSTEM
K250112 FitboneTM Trochanteric
K242270 OrthoNext Platform System
K242861 TrueLok Elevate
K233867 Fitbone Trochanteric
K232648 RODEO Telescopic Nail
K232169 FITBONE® Transport and Lengthening System
K213572 JuniOrtho Plating System™
K212044 TrueLok Evo
K210157 SOLE Medial Column Fusion Plate
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