Cleared Traditional

K143355 - The Simple Locking IntraMedullary (SLIM) System (FDA 510(k) Clearance)

Jul 2015
Decision
228d
Days
Class 2
Risk

K143355 is an FDA 510(k) clearance for the The Simple Locking IntraMedullary (SLIM) System. This device is classified as a Rod, Fixation, Intramedullary And Accessories (Class II - Special Controls, product code HSB).

Submitted by Pega Medical, Inc. (Laval, CA). The FDA issued a Cleared decision on July 10, 2015, 228 days after receiving the submission on November 24, 2014.

This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3020.

Submission Details

510(k) Number K143355 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 24, 2014
Decision Date July 10, 2015
Days to Decision 228 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF

Device Classification

Product Code HSB - Rod, Fixation, Intramedullary And Accessories
Device Class Class II - Special Controls
CFR Regulation 21 CFR 888.3020