Cleared Traditional

K141228 - AOS 6.5MM CAPTURED, FULLY THREADED CANCELLOUS SCREW (FDA 510(k) Clearance)

Jul 2014
Decision
57d
Days
Class 2
Risk

K141228 is an FDA 510(k) clearance for the AOS 6.5MM CAPTURED, FULLY THREADED CANCELLOUS SCREW. This device is classified as a Rod, Fixation, Intramedullary And Accessories (Class II - Special Controls, product code HSB).

Submitted by Advanced Orthopaedic Solutions, Inc. (Torrance, US). The FDA issued a Cleared decision on July 8, 2014, 57 days after receiving the submission on May 12, 2014.

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

Submission Details

510(k) Number K141228 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 12, 2014
Decision Date July 08, 2014
Days to Decision 57 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