Cleared Traditional

K201253 - Modular Rail System, TAYLOR SPATIAL FRAME External Fixator, JET-X Fixator, ILIZAROV External Fixator, Other External Fixation
(FDA 510(k) Clearance)

Dec 2020
Decision
211d
Days
Class 2
Risk

K201253 is an FDA 510(k) clearance for the Modular Rail System, TAYLOR SPATIAL FRAME External Fixator, JET-X Fixator, ILIZAROV External Fixator, Other External Fixation. This device is classified as a Appliance, Fixation, Nail/blade/plate Combination, Multiple Component (Class II - Special Controls, product code KTT).

Submitted by Smith & Nephew (Memphis, US). The FDA issued a Cleared decision on December 8, 2020, 211 days after receiving the submission on May 11, 2020.

This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3030.

Submission Details

510(k) Number K201253 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 11, 2020
Decision Date December 08, 2020
Days to Decision 211 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF

Device Classification

Product Code KTT — Appliance, Fixation, Nail/blade/plate Combination, Multiple Component
Device Class Class II - Special Controls
CFR Regulation 21 CFR 888.3030

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