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FDA 510(k)

VersaLift Expandable System

K-Number: K260837 · 2026-05-12

ApplicantLife Spine, Inc.
Decision Date2026-05-12
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VersaLift Expandable System is a medical device manufactured by Life Spine, Inc.. It received FDA 510(k) clearance on 2026-05-12 under approval number K260837. 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 VersaLift Expandable System?

VersaLift Expandable System is a medical device that received FDA 510(k) clearance on 2026-05-12. It is manufactured by Life Spine, Inc.. The 510(k) number is K260837.

When was VersaLift Expandable System approved by the FDA?

VersaLift Expandable System received FDA 510(k) clearance on 2026-05-12, under approval number K260837.

What company makes VersaLift Expandable System?

VersaLift Expandable System is manufactured by Life Spine, Inc..

What is the FDA product code for VersaLift Expandable System?

The FDA product code for VersaLift Expandable System is MAX.

Related Devices (Code: MAX)

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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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