EVOS Small Fragment Plating System

FDA 510(k) K172262 · Smith & Nephew, Inc.

Substantially Equivalent

510(k) numberK172262

Submission

Device name
EVOS Small Fragment Plating System
Applicant
Smith & Nephew, Inc.
Memphis, TN, US
Received
July 27, 2017
Decision date
August 23, 2017
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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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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K251627BIORAPTOR 2.3 PK Suture Anchor w/ ULTRABRAID (#2) Suture (cobraid blue); BIORAPTOR 2.3…MBI · Special 06/25/2025SE
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K250677LEGION Total Knee SystemJWH · Special 04/02/2025SE
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K241666EVOS Pelvic and Acetabular SystemHRS · Traditional 02/19/2025SE

Questions and answers

When was EVOS Small Fragment Plating System cleared by the FDA?

EVOS Small Fragment Plating System (K172262) received a 510(k) decision of Substantially Equivalent on August 23, 2017, 27 days after the submission was received.

What is the product code of K172262?

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