Pediatric Nailing Platform Tibia

FDA 510(k) K231266 · OrthoPediatrics Corp.

Substantially Equivalent

510(k) numberK231266

Submission

Device name
Pediatric Nailing Platform Tibia
Applicant
OrthoPediatrics Corp.
Warsaw, IN, US
Received
May 2, 2023
Decision date
August 21, 2023
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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K261043AUTOBAHN™ Nailing SystemHSB · Special Globus Medical, Inc.04/24/2026SE
K252016Arthrex Humeral NailsHSB · Traditional Arthrex, Inc.03/20/2026SE
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K250623Pediatric Nailing Platform Tibia Pediatric Nailing Platform FemurHSB · Special 04/01/2025SE
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K233105RESPONSE™ Rib and Pelvic SystemMDI · Traditional 01/20/2024SE
K222105RESPONSE 5.5/6.0 Cannulated Screw SystemNKB · Special 03/23/2023SE
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Questions and answers

When was Pediatric Nailing Platform Tibia cleared by the FDA?

Pediatric Nailing Platform Tibia (K231266) received a 510(k) decision of Substantially Equivalent on August 21, 2023, 111 days after the submission was received.

What is the product code of K231266?

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