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CATALYFT™ PL
 Expandable Titanium Interbody Device for PLIF, TLIF and MIDLF Procedures

Catalyft™ PL expandable interbody system creates expansion at the precise angle and lift you need for minimally invasive, patient specific solutions while streamlining workflow with a powerful integration of different solutions that perfectly work together.1

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Catalyft PL expandable titanium interbody device

Overview

Lift. Align. Transform

Discover Catalyft™ expansion technology

Available in two footprints - PL and PL 40 - the Catalyft™ PL expandable interbody system features1:

  • a unique design for anterior rim engagement.
  • a beveled tip for ease of insertion.
  • seamless integration with StealthStation™ Navigation System.
  • simplified bone graft delivery.
  • an active expansion at the precise angle and lift you need for minimally invasive, patient-specific solutions to meet your sagittal alignment goals.

 

Product Details

Two footprints available

Catalyft PL Product image

Catalyft™ PL

Designed for TLIF, PLIF and MIDLF procedures, the titanium Catalyft™ PL expandable interbody features increased length and continuous adjustment up to 22o of lordosis.2 Unique shapes allow optimal positioning and improved anterior rim engagement to minimize the risk of subsidence to aid in neuroforaminal decompression.1 The grit blasted, titanium surface contributes to implant anti migration and osteoconduction.3

Catalyft PL 40 product image

Catalyft™ PL40

Building upon the unique benefits of Catalyft™ PL, the titanium Catalyft™ PL40 expandable interbody provides 40% more surface area distally compared to the Catalyft™ PL implant, which allows for increased anterior rim contact to reduce the risk of subsidence.1 The anatomic beveled tip allows for greater apophyseal ring contact and ease of insertion.4


 

Clear visualization with active expansion technology

Catalyft navigation films

Catalyft™ PL Expandable Interbody System seamlessly integrates with StealthStation™ Navigation, enabling real time visualization and streamlined workflow to support minimally invasive procedures.1

StealthStation™ Navigation features Virtual Expansion Technology, offering the ability to see the Catalyft™ PL and PL40 implants implant in both collapsed and expanded positions prior to implantation to optimize surgical planning.1

All-in-one Bone Graft delivery

Step 2: Catalyft and Inject DBF Bone Graft Insertion

Seamlessly integraded Bone Graft delivery

The integrated design of Catalyft™ PL expandable interbody system and Grafton™ DBF inject* streamlines the workflow and precisely delivers bone graft.1

Grafton™ DBF Inject* boosts seamless fusion by flowing through the inserter and expanded implant to completely fill the disc space.

*Grafton™ DBF Inject can be used with the Catalyft™ PL Expandable Interbody System when hydrated with bone marrow aspirate (BMA).

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1

Medtronic Internal Report: Catalyft ™PL Implant/Instrument Design Validation (Anatomical and Navigation Simulated Use) Report. Document GC17012_TP_007 RPT, version B. Revision date: 02 05 2021

2

Medtronic Internal Report: 6068073/9116 - C82886, rev B. Revision date: 05 07 2021

3

Medtronic Internal Report: 6068073/8116 01 C81951, rev A. Date: 20 01 2021. Medtronic Internal Report: 6068073/8116 02 C81951, rev A. Date: 20 01 2021.

4

Medtronic Internal Report: Catalyft PL Tip Design Rationale - GC17012_GM_044, rev. A. Revision Date:07 21 2021.

See the device manual for information regarding the instructions for use, indications, contraindications, warnings, precautions, and potential adverse events. For further information, contact your local Medtronic representative and/or consult the Medtronic website at medtronic.eu.

For applicable products, consult instructions for use on manuals.medtronic.com. Manuals can be viewed using a current version of any major internet browser. For best results, use Adobe Acrobat® Reader with the browser.

This information intended only for users in markets where Medtronic products and therapies are approved or available for use as indicated within the respective product manuals. Content on specific Medtronic products and therapies is not intended for users in markets that do not have authorization for use.