OsteoMed ExtremiLOCK Wrist Plating System

FDA 510(k) K161041 · Osteomed

Substantially Equivalent

510(k) numberK161041

Submission

Device name
OsteoMed ExtremiLOCK Wrist Plating System
Applicant
Osteomed
Addison, TX, US
Received
April 13, 2016
Decision date
May 19, 2016
Decision
Substantially Equivalent (SESE)
Type
Special 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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K261647Tempo Plating System; Ultra Compression Screw SystemHRS · Traditional Pace Surgical09/03/2026SE
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K262537Versalock Sterile Plating SystemHRS · Special GM Dos Reis Industria e Comercio Ltda.08/19/2026SE
K260277Mikron Trauma Bone Plate& Screw SystemHRS · Traditional Mikron Makina San. ve Tic. Ltd. Sti.08/13/2026SE
K261511Xpert AnkleHRS · Traditional Newclip Technics07/28/2026SE
K261406Versalock Proximal Tibial Plating SystemHRS · Traditional GM Dos Reis Industria e Comercio Ltda.07/21/2026SE
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

510(k)DeviceDecision
K212570OsteoPlan SystemDZJ · Traditional 02/11/2022SE
K203479ExtremiLOCK Lateral Ankle Fusion PlatesHRS · Traditional 02/24/2021SE
K202105OsteoMed ExtremiFix Mini & Small System TrayKCT · Traditional 10/29/2020SE
K202680OsteoMed ExtremiFix Mini & Small Cannulated Screw SystemHWC · Special 10/15/2020SE
K173391OsteoMed QuickFix Hybrid MMF Sterilization TrayKCT · Traditional 05/10/2018SE
K162542OsteoMed PINNACLE DriverHBE · Traditional 05/19/2017SE
K163303OsteoMed ExtremiFix Mid and Large Screw SystemHWC · Traditional 04/04/2017SE
K162544OsteoMed PINNACLE DriverKMW · Traditional 04/04/2017SE
K152145OsteoMed ExtremiLOCK Wrist Plating SystemHRS · Traditional 12/21/2015SE
K151195OsteoMed IMF ScrewDZL · Traditional 09/21/2015SE

Questions and answers

When was OsteoMed ExtremiLOCK Wrist Plating System cleared by the FDA?

OsteoMed ExtremiLOCK Wrist Plating System (K161041) received a 510(k) decision of Substantially Equivalent on May 19, 2016, 36 days after the submission was received.

What is the product code of K161041?

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