Agile Nail

FDA 510(k) K172699 · Orthofix Srl

Substantially Equivalent

510(k) numberK172699

Submission

Device name
Agile Nail
Applicant
Orthofix Srl
Bussolengo, IT
Received
September 7, 2017
Decision date
April 23, 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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K253046HERA Interlocking Intramedullary Nailing SystemHSB · Traditional ZheJiang Decans Medical Devices Co., Ltd.06/16/2026SE
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
K252961Fusion FibFix NailHSB · Traditional Fusion Orthopedics USA, LLC03/18/2026SE

More from Fusion Orthopedics USA, LLC

510(k)DeviceDecision
K260146Fitbone® Transport and Lengthening SystemHSB · Traditional 05/19/2026SE
K253991Fitbone™ Trochanteric, FITBONE® Transport and Lengthening System, FITBONE® TAAHSB · Traditional 05/08/2026SE
K250112FitboneTM TrochantericHSB · Traditional 04/10/2025SE
K242270OrthoNext Platform SystemQIH · Traditional 12/19/2024SE
K242861TrueLok ElevateKTT · Traditional 12/03/2024SE
K233867Fitbone TrochantericHSB · Traditional 06/18/2024SE
K240749PILLAR SA Ti Spacer System (82-XXX)MAX · Traditional 05/28/2024SE
K232648RODEO Telescopic NailHSB · Traditional 05/03/2024SE
K232169FITBONE® Transport and Lengthening SystemHSB · Traditional 03/22/2024SE
K213572JuniOrtho Plating System™HWC · Traditional 01/18/2022SE

Questions and answers

When was Agile Nail cleared by the FDA?

Agile Nail (K172699) received a 510(k) decision of Substantially Equivalent on April 23, 2018, 228 days after the submission was received.

What is the product code of K172699?

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