FDA 510(k)

Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer System

Numéro K : K253748 · 2026-01-23

Date de décision2026-01-23

Code produitMAX

Comité consultatifOR

DécisionSubstantially Equivalent

Résumé du dispositif

Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer System is the device name listed in this FDA 510(k) record. The listed applicant is Life Spine, Inc.. It received FDA 510(k) clearance on 2026-01-23 under 510(k) number K253748. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer System?

Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer System is a medical device that received FDA 510(k) clearance on 2026-01-23. The listed applicant is Life Spine, Inc.. The 510(k) number is K253748.

When did Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer System receive FDA 510(k) clearance?

Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer System received FDA 510(k) clearance on 2026-01-23, under 510(k) number K253748.

Who is the listed applicant for Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer System?

The FDA 510(k) record lists Life Spine, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer System?

The FDA product code for Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer System is MAX.

Essais cliniques associés

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Dispositifs connexes (Code : MAX)

K261049SCALA® TLSpineart SA K261430TruLift Expandable SystemLife Spine, Inc.K253011Catalyft PL Expandable Interbody SystemMedtronic Sofamor Danek USA, Inc.K261020Symmetrix™ L Spinal SystemMedtronic Sofamor Danek USA, Inc.K253420Admiral ACP System; Explorer TO System; Laminoplasty System; Manta Ray TDF Spacer; Meridian Interbody System; Meridian Anterior Plate System; Reef L Interbody System; Reef TO/TA System; Regatta Lateral System; Regatta Lateral Plate System; Shoreline ACS Interbody System; Shoreline Threaded TruProfile Plate; Shoreline RT Interbody System; Vu Mesh; WaveForm A Interbody System; WaveForm C Interbody System; WaveForm L Interbody System; WaveForm TA Interbody System; WaveForm TO Interbody SySeaSpine Orthopedics Corporation K253151Système de Cage de Fusion Intervertébral FuleBeijing Fule Science & Technology Development Co., Ltd.

Source officielle

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