FDA 510(k)

ProLift Micro Expandable Spacer System

K-Number: K223430 · 2023-05-04

Decision Date2023-05-04

Product CodeMAX

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

ProLift Micro Expandable Spacer System is a medical device manufactured by Life Spine, Inc.. It received FDA 510(k) clearance on 2023-05-04 under approval number K223430. 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 ProLift Micro Expandable Spacer System?

ProLift Micro Expandable Spacer System is a medical device that received FDA 510(k) clearance on 2023-05-04. It is manufactured by Life Spine, Inc.. The 510(k) number is K223430.

When was ProLift Micro Expandable Spacer System approved by the FDA?

ProLift Micro Expandable Spacer System received FDA 510(k) clearance on 2023-05-04, under approval number K223430.

What company makes ProLift Micro Expandable Spacer System?

ProLift Micro Expandable Spacer System is manufactured by Life Spine, Inc..

What is the FDA product code for ProLift Micro Expandable Spacer System?

The FDA product code for ProLift Micro Expandable Spacer System is MAX.

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Other Devices by Life Spine, Inc.

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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.