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

EBA One Nailing System

K Number: K183666 · Decision Nov 14, 2019
Classifications
1
FEI Numbers
302
Registration Numbers
302
Same Product Code
528
Applicant Total
8
Review Days
322

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
EBA One Nailing System
K Number
K183666
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3020
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Citieffe S.R.L.
Date Received
December 27, 2018
Decision Date
November 14, 2019
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HSB), ordered by most recent decision date.

View all

Other Clearances by Citieffe S.R.L.

K Number Device Name
K250197 Estremo Fibular Nail
K181540 Estremo Citieffe Nailing System
K180150 PL8 Wrist Reconstruction Plate
K163323 Dolphix® External Fixation System MR Conditional
K150661 ST.A.R. 90 F4 External Fixation Screws With Hydroxyapatite
K132363 DOLPHIX EXTERNAL FIXATION SYSTEM
K131005 EBA2 FEMORAL NAILING SYSTEM