Lima-Lio SMR Shoulder System - Humeral Stems, Lima-Lio SMR Shoulder System - Humeral Bodies,

FDA 510(k) K100858 · Lima-Lto S.P.A.

Substantially Equivalent

510(k) numberK100858

Submission

Device name
Lima-Lio SMR Shoulder System - Humeral Stems, Lima-Lio SMR Shoulder System - Humeral Bodies,
Applicant
Lima-Lto S.P.A.
Winona Lake, IN, US
Received
March 26, 2010
Decision date
December 10, 2010
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KWT – Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3650
Specialty
Orthopedic
Implant
Yes

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More from Fx Shoulder USA, Inc.

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K101263Lima-Lto SMR Shoulder System - Finned Humeral Stems, Lima-Lto SMR Shoulder System -…KWT · Traditional 01/28/2011SE

Questions and answers

When was Lima-Lio SMR Shoulder System - Humeral Stems, Lima-Lio SMR Shoulder System - Humeral Bodies, cleared by the FDA?

Lima-Lio SMR Shoulder System - Humeral Stems, Lima-Lio SMR Shoulder System - Humeral Bodies, (K100858) received a 510(k) decision of Substantially Equivalent on December 10, 2010, 259 days after the submission was received.

What is the product code of K100858?

The FDA product code is KWT – Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented, a Class II (moderate risk) device regulated under 21 CFR 888.3650.