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FDA 510(k)

TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System

K-Number: K251502 · 2025-07-07

ApplicantLife Spine, Inc.
Decision Date2025-07-07
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System is a medical device manufactured by Life Spine, Inc.. It received FDA 510(k) clearance on 2025-07-07 under approval number K251502. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System?

TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System is a medical device that received FDA 510(k) clearance on 2025-07-07. It is manufactured by Life Spine, Inc.. The 510(k) number is K251502.

When was TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System approved by the FDA?

TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System received FDA 510(k) clearance on 2025-07-07, under approval number K251502.

What company makes TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System?

TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System is manufactured by Life Spine, Inc..

What is the FDA product code for TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System?

The FDA product code for TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System is MAX.

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Other Devices by Life Spine, Inc.

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Related Devices (Code: MAX)

K163180Hubble IIOrbbo Surgical, LLC K162446FORZA Spacer System, PILLAR PEEK Spacer System, PILLAR SA PEEK Spacer System, SKYHAWK Lateral Interbody Fusion SystemOrthofix, Inc. K162327COUGAR® LS Lateral Cage System and COUGAR® SystemMedos International SARL K162103Choice Spine Lumbar Spacer System (Sabre™, Shark™, Hornet™, Harpoon™), Choice Spine Interbody Fusion System (Harrier™), Choice Spine Vertebral Body Replacement System (Hawkeye™)Choicespine, LP K162431Luna 3D Interbody Fusion SystemBenvenue Medical, Inc. K160959Xsert Lumbar Expandable Interbody SystemX-Spine Systems, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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