VERTA Corpectomy Cage

FDA 510(k) K143490 · Camber Spine

Substantially Equivalent

510(k) numberK143490

Submission

Device name
VERTA Corpectomy Cage
Applicant
Camber Spine
Wayne, PA, US
Received
December 8, 2014
Decision date
January 26, 2015
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

Other 510(k)s with product code MQP

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K261810Vertiwedge® Intraosseous SystemMQP · Special Foundation Surgical Group07/31/2026SE
K261031Poseidon STMQP · Traditional Signus Medinzintechnik GmbH07/10/2026SE
K253158VyBrate™ VBR SystemMQP · Traditional Vy Spine, LLC01/07/2026SE
K241468Vertiwedge® Intraosseous SystemMQP · Traditional Foundation Surgical Group, Inc.11/07/2024SE
K232790KONG®-TL VBR System and KONG® C VBR SystemMQP · Traditional Icotec AG04/04/2024SE
K233359DOMINION Expandable Corpectomy SystemMQP · Traditional Astura Medical03/08/2024SE
K231134VerteLoc Spinal SystemMQP · Traditional Signature Orthopaedics Pty, Ltd.02/13/2024SE
K232173Ascend VBR System, Ascend NanoTec VBR SystemMQP · Traditional Alphatec Spine, Inc.10/06/2023SE
K211892ArtFx Corpectomy Cages (Espinax and Distractania Corpectomy Cages)MQP · Traditional Arftx Medical, LLC10/06/2022SE
K202637F3D Corpectomy SystemMQP · Traditional Corelink, LLC12/23/2020SE

More from Corelink, LLC

510(k)DeviceDecision
K133366Orthros Posterior Stabilization SystemNKB · Traditional 04/08/2014SE
K134038Camber Spine Diagon Oblique CageMAX · Special 03/20/2014SE
K133529Camber Spine Coveris Cervical CageODP · Traditional 03/20/2014SE

Questions and answers

When was VERTA Corpectomy Cage cleared by the FDA?

VERTA Corpectomy Cage (K143490) received a 510(k) decision of Substantially Equivalent on January 26, 2015, 49 days after the submission was received.

What is the product code of K143490?

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