I.T.S. Extremity Fixation Systems

FDA 510(k) K131722 · I.T.S. GmbH

Substantially Equivalent

510(k) numberK131722

Submission

Device name
I.T.S. Extremity Fixation Systems
Applicant
I.T.S. GmbH
Prior Lake, MN, US
Received
June 12, 2013
Decision date
August 7, 2013
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
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More from Bonebridge AG

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K260958I.T.S. Clavicle Plates with Angular Stability; I.T.S. Volar Radius Plate with Angular…HRS · Traditional 06/16/2026SE
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K233134I.T.S. INS Proximal Femur NailHSB · Traditional 02/12/2024SE
K210935I.T.S. Pelvic Reconstruction System (PRS RX & PRS Phoenix)HRS · Traditional 08/31/2022SE
K142418I.T.S. Hand Locking Plates System - HLSHRS · Traditional 09/26/2014SE
K132945Cfn-Cannulated Femur Nail, Ctn-Cannulated Tibia Nail, Chn-Cannulated Humeral NailHSB · Traditional 03/07/2014SE
K130008Distal Ulna Locking Plate (Dul), Ulna Osteotomy Locking Plate (Uol), 3.0 Cancellous…HRS · Traditional 06/25/2013SE

Questions and answers

When was I.T.S. Extremity Fixation Systems cleared by the FDA?

I.T.S. Extremity Fixation Systems (K131722) received a 510(k) decision of Substantially Equivalent on August 7, 2013, 56 days after the submission was received.

What is the product code of K131722?

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