Lima-Lto SMR Shoulder System - Finned Humeral Stems, Lima-Lto SMR Shoulder System - Finned Humeral Bodies,

FDA 510(k) K101263 · Lima-Lto S.P.A.

Substantially Equivalent

510(k) numberK101263

Submission

Device name
Lima-Lto SMR Shoulder System - Finned Humeral Stems, Lima-Lto SMR Shoulder System - Finned Humeral Bodies,
Applicant
Lima-Lto S.P.A.
Winona Lake, IN, US
Received
May 5, 2010
Decision date
January 28, 2011
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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K241944AGILON® XO Shoulder Replacement SystemKWT · Traditional Implantcast GmbH03/10/2025SE
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K223631Comprehensive Segmental Revision System(SRS)KWT · Traditional Biomet Orthopedics07/12/2023SE
K222482AGILON XO Shoulder SystemKWT · Traditional Implantcast GmbH09/28/2022SE
K210899LINK Embrace Shoulder System- Anatomical ConfigurationKWT · Traditional Waldemar Link GmbH & Co. KG06/21/2021SE
K191698TiN Coated Humeral HeadKWT · Traditional Fx Shoulder USA, Inc.07/16/2020SE

More from Fx Shoulder USA, Inc.

510(k)DeviceDecision
K100858Lima-Lio SMR Shoulder System - Humeral Stems, Lima-Lio SMR Shoulder System - Humeral…KWT · Traditional 12/10/2010SE

Questions and answers

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

Lima-Lto SMR Shoulder System - Finned Humeral Stems, Lima-Lto SMR Shoulder System - Finned Humeral Bodies, (K101263) received a 510(k) decision of Substantially Equivalent on January 28, 2011, 268 days after the submission was received.

What is the product code of K101263?

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.