Apex Femoral Nailing System

FDA 510(k) K181375 · Orthoxel

Substantially Equivalent

510(k) numberK181375

Submission

Device name
Apex Femoral Nailing System
Applicant
Orthoxel
Bishopstown, IE
Received
May 24, 2018
Decision date
July 17, 2018
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HSB – Rod, Fixation, Intramedullary And Accessories
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3020
Specialty
Orthopedic
Implant
Yes

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K260146Fitbone® Transport and Lengthening SystemHSB · Traditional Orthofix Srl05/19/2026SE
K253991Fitbone™ Trochanteric, FITBONE® Transport and Lengthening System, FITBONE® TAAHSB · Traditional Orthofix Srl05/08/2026SE
K261043AUTOBAHN™ Nailing SystemHSB · Special Globus Medical, Inc.04/24/2026SE
K252016Arthrex Humeral NailsHSB · Traditional Arthrex, Inc.03/20/2026SE
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More from Fusion Orthopedics USA, LLC

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K170972Apex Tibial Nailing SystemHSB · Traditional 12/20/2017SE

Questions and answers

When was Apex Femoral Nailing System cleared by the FDA?

Apex Femoral Nailing System (K181375) received a 510(k) decision of Substantially Equivalent on July 17, 2018, 54 days after the submission was received.

What is the product code of K181375?

The FDA product code is HSB – Rod, Fixation, Intramedullary And Accessories, a Class II (moderate risk) device regulated under 21 CFR 888.3020.