T2 STRATOSPHERE™ Expandable Corpectomy System

FDA 510(k) K181328 · Medtronic Sofamor Danek USA, Inc.

Substantially Equivalent

510(k) numberK181328

Submission

Device name
T2 STRATOSPHERE™ Expandable Corpectomy System
Applicant
Medtronic Sofamor Danek USA, Inc.
Memphis, TN, US
Received
May 18, 2018
Decision date
September 19, 2018
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MQP – Spinal Vertebral Body Replacement Device
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3060
Specialty
Orthopedic
Implant
Yes

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K233359DOMINION Expandable Corpectomy SystemMQP · Traditional Astura Medical03/08/2024SE
K231134VerteLoc Spinal SystemMQP · Traditional Signature Orthopaedics Pty, Ltd.02/13/2024SE
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K211892ArtFx Corpectomy Cages (Espinax and Distractania Corpectomy Cages)MQP · Traditional Arftx Medical, LLC10/06/2022SE
K202637F3D Corpectomy SystemMQP · Traditional Corelink, LLC12/23/2020SE

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Questions and answers

When was T2 STRATOSPHERE™ Expandable Corpectomy System cleared by the FDA?

T2 STRATOSPHERE™ Expandable Corpectomy System (K181328) received a 510(k) decision of Substantially Equivalent on September 19, 2018, 124 days after the submission was received.

What is the product code of K181328?

The FDA product code is MQP – Spinal Vertebral Body Replacement Device, a Class II (moderate risk) device regulated under 21 CFR 888.3060.