Fusion Medical Ring Lock System

FDA 510(k) K100857 · John J Riccio

Substantially Equivalent

510(k) numberK100857

Submission

Device name
Fusion Medical Ring Lock System
Applicant
John J Riccio
West Haven, CT, US
Received
March 26, 2010
Decision date
May 27, 2010
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KTT – Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3030
Specialty
Orthopedic
Implant
Yes

Other 510(k)s with product code KTT

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K254087MAXFRAME AUTOSTRUT™ with Bluetooth Multi-Axial Correction SystemKTT · Traditional Synthes (USA) Products, LLC06/11/2026SE
K260900DYNEX® External Fixation SystemsKTT · Special Vilex, LLC04/17/2026SE
K260112QuikFix External Fixator: Knee-Spanning PackKTT · Traditional Stabiliz Orthopaedics, Inc.03/23/2026SE
K253291Excelsior SystemKTT · Traditional Blue Ocean Global01/20/2026SE
K253613Monkey Rings External Ring Fixation SystemKTT · Special Paragon 28, Inc.12/19/2025SE
K253202Hoffmann LRF SystemKTT · Traditional Stryker GmbH12/19/2025SE
K252555Medusa Orthopedics Boa External Fixation SystemKTT · Traditional Medusa Orthopedics, LLC11/25/2025SE
K252625The Response Ortho Smart Fixator - Hexapod SystemKTT · Traditional Response Ortho Solutions, LLC11/20/2025SE
K252106External Fixation Mini Rail SystemKTT · Traditional Paragon 28, Inc.09/30/2025SE
K251862External Fixation Bone DistractorKTT · Traditional Paragon 28, Inc.08/11/2025SE

Questions and answers

When was Fusion Medical Ring Lock System cleared by the FDA?

Fusion Medical Ring Lock System (K100857) received a 510(k) decision of Substantially Equivalent on May 27, 2010, 62 days after the submission was received.

What is the product code of K100857?

The FDA product code is KTT – Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, a Class II (moderate risk) device regulated under 21 CFR 888.3030.