Orthopediatrics Pediplates System

FDA 510(k) K081407 · OrthoPediatrics Corp.

Substantially Equivalent

510(k) numberK081407

Submission

Device name
Orthopediatrics Pediplates System
Applicant
OrthoPediatrics Corp.
Warsaw, IN, US
Received
May 19, 2008
Decision date
July 22, 2008
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HRS – Plate, Fixation, Bone
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3030
Specialty
Orthopedic
Implant
Yes

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K262032TriMed Non-Spanning Wrist Fusion Plates (NSFL-STD);TriMed Non-Spanning Wrist Fusion…HRS · Special TriMed, Inc.07/16/2026SE
K261191Alians Elbow SHRS · Traditional Newclip Technics07/08/2026SE
K261054RibPlate SystemHRS · Traditional Stryker Leibinger GmbH & Co KG07/01/2026SE
K261351SALGINA 2.5mm Distal Radius SystemHRS · Traditional Bonebridge AG06/26/2026SE

More from Bonebridge AG

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K251362PediFlex™ Flexible Nail SystemHTY · Traditional 06/24/2025SE
K243963Pediatric Plating Platform HipHRS · Traditional 04/29/2025SE
K250623Pediatric Nailing Platform Tibia Pediatric Nailing Platform FemurHSB · Special 04/01/2025SE
K241816VerteGlide Spinal Growth Guidance SystemPGM · Traditional 03/14/2025SE
K243798Orthex External Fixation SystemKTT · Traditional 03/07/2025SE
K233105RESPONSE™ Rib and Pelvic SystemMDI · Traditional 01/20/2024SE
K231266Pediatric Nailing Platform TibiaHSB · Traditional 08/21/2023SE
K222105RESPONSE 5.5/6.0 Cannulated Screw SystemNKB · Special 03/23/2023SE

Questions and answers

When was Orthopediatrics Pediplates System cleared by the FDA?

Orthopediatrics Pediplates System (K081407) received a 510(k) decision of Substantially Equivalent on July 22, 2008, 64 days after the submission was received.

What is the product code of K081407?

The FDA product code is HRS – Plate, Fixation, Bone, a Class II (moderate risk) device regulated under 21 CFR 888.3030.