Baby Gorilla/Gorilla Plating System

FDA 510(k) K190365 · Paragon 28, Inc.

Substantially Equivalent

510(k) numberK190365

Submission

Device name
Baby Gorilla/Gorilla Plating System
Applicant
Paragon 28, Inc.
Englewood, CO, US
Received
February 15, 2019
Decision date
April 12, 2019
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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K262047Grappler Suture Anchor SystemMBI · Special 08/03/2026SE
K253886Grappler Suture Anchor PCFD Tether SystemMBI · Traditional 03/17/2026SE
K253591Phantom® Hindfoot TTC/TC Nail SystemHSB · Traditional 03/05/2026SE
K253613Monkey Rings External Ring Fixation SystemKTT · Special 12/19/2025SE
K252106External Fixation Mini Rail SystemKTT · Traditional 09/30/2025SE
K251862External Fixation Bone DistractorKTT · Traditional 08/11/2025SE
K250952Baby Gorilla®/Gorilla® Plating SystemHRS · Traditional 07/18/2025SE
K251850Phantom® Hindfoot TTC/TC Nail SystemHSB · Special 07/14/2025SE

Questions and answers

When was Baby Gorilla/Gorilla Plating System cleared by the FDA?

Baby Gorilla/Gorilla Plating System (K190365) received a 510(k) decision of Substantially Equivalent on April 12, 2019, 56 days after the submission was received.

What is the product code of K190365?

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