TEMA Elbow system - Line extension

FDA 510(k) K222807 · Lima Corporate S.P.A.

Substantially Equivalent

510(k) numberK222807

Submission

Device name
TEMA Elbow system - Line extension
Applicant
Lima Corporate S.P.A.
Villanova Di San Daniele Del Friuli, IT
Received
September 16, 2022
Decision date
October 26, 2022
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JDB – Prosthesis, Elbow, Semi-Constrained, Cemented
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3160
Specialty
Orthopedic
Implant
Yes

Other 510(k)s with product code JDB

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K193247LATITUDE EV™ Total Elbow ArthroplastyJDB · Traditional Tornier, Inc.08/05/2020SE
K182461LATITUDE EV Total Elbow ArthroplastyJDB · Traditional Tornier, Inc.12/27/2018SE
K171010Latitude EV Total Elbow ArthroplastyJDB · Traditional Tornier, Inc.08/31/2017SE
K102180Rhead Radial Head Extended StemsJDB · Traditional Small Bone Innovations, Inc.12/20/2010SE
K100562Latitude Elbow ProsthesisJDB · Special Tornier, Inc.06/29/2010SE
K070787Latitude Elbow ProthesisJDB · Special Tornier08/24/2007SE
K070236Sbi Lateral Radio CapitellumJDB · Special Small Bone Innovations, Inc.02/21/2007SE
K060438RHSJDB · Traditional Tornier04/18/2006SE
K060038Sbi Radio-Capitellar ImplantJDB · Traditional Small Bone Innovations, Inc.03/30/2006SE
K050848Tornier Elbow ProsthesisJDB · Traditional Tornier07/14/2005SE

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Questions and answers

When was TEMA Elbow system - Line extension cleared by the FDA?

TEMA Elbow system - Line extension (K222807) received a 510(k) decision of Substantially Equivalent on October 26, 2022, 40 days after the submission was received.

What is the product code of K222807?

The FDA product code is JDB – Prosthesis, Elbow, Semi-Constrained, Cemented, a Class II (moderate risk) device regulated under 21 CFR 888.3160.