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

Estremo Fibular Nail

K Number: K250197 · Decision Oct 17, 2025
Classifications
1
FEI Numbers
302
Registration Numbers
302
Same Product Code
528
Applicant Total
8
Review Days
267

Basic Information

Device Name
Estremo Fibular Nail
K Number
K250197
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3020
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Citieffe S.R.L.
Date Received
January 23, 2025
Decision Date
October 17, 2025
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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