Cleared Traditional

K140676 - PROFEMUR TL CLASSIC LONG NECK HIP STEMS (FDA 510(k) Clearance)

May 2014
Decision
73d
Days
Class 2
Risk

K140676 is an FDA 510(k) clearance for the PROFEMUR TL CLASSIC LONG NECK HIP STEMS. This device is classified as a Prosthesis, Hip, Semi-constrained, Metal/ceramic/polymer, Cemented Or Non-porous, Uncemented (Class II - Special Controls, product code LZO).

Submitted by Microport Orthopedics, Inc. (Arlington, US). The FDA issued a Cleared decision on May 30, 2014, 73 days after receiving the submission on March 18, 2014.

This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3353.

Submission Details

510(k) Number K140676 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 18, 2014
Decision Date May 30, 2014
Days to Decision 73 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF

Device Classification

Product Code LZO — Prosthesis, Hip, Semi-constrained, Metal/ceramic/polymer, Cemented Or Non-porous, Uncemented
Device Class Class II - Special Controls
CFR Regulation 21 CFR 888.3353

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