Modular Rail System, TAYLOR SPATIAL FRAME External Fixator, JET-X Fixator, ILIZAROV External Fixator, Other External Fixation

FDA 510(k) K201253 · Smith & Nephew

Substantially Equivalent

510(k) numberK201253

Submission

Device name
Modular Rail System, TAYLOR SPATIAL FRAME External Fixator, JET-X Fixator, ILIZAROV External Fixator, Other External Fixation
Applicant
Smith & Nephew
Cordova, TN, US
Received
May 11, 2020
Decision date
December 8, 2020
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

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K251862External Fixation Bone DistractorKTT · Traditional Paragon 28, Inc.08/11/2025SE

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K243608TRIGEN Stable Lock Nut & WasherJDS · Traditional 06/12/2025SE
K250677LEGION Total Knee SystemJWH · Special 04/02/2025SE
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Questions and answers

When was Modular Rail System, TAYLOR SPATIAL FRAME External Fixator, JET-X Fixator, ILIZAROV External Fixator, Other External Fixation cleared by the FDA?

Modular Rail System, TAYLOR SPATIAL FRAME External Fixator, JET-X Fixator, ILIZAROV External Fixator, Other External Fixation (K201253) received a 510(k) decision of Substantially Equivalent on December 8, 2020, 211 days after the submission was received.

What is the product code of K201253?

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.