Single/Multiple Component Metallic Bone Fixation

FDA 510(k) K860600 · 3M Company

Substantially Equivalent

510(k) numberK860600

Submission

Device name
Single/Multiple Component Metallic Bone Fixation
Applicant
3M Company
Cottae Grove, MN, US
Received
February 19, 1986
Decision date
March 13, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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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

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Questions and answers

When was Single/Multiple Component Metallic Bone Fixation cleared by the FDA?

Single/Multiple Component Metallic Bone Fixation (K860600) received a 510(k) decision of Substantially Equivalent on March 13, 1986, 22 days after the submission was received.

What is the product code of K860600?

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