FDA 510(k)

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

Número K: K253748 · 2026-01-23

Data da decisão2026-01-23

Código do produtoMAX

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

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.

Perguntas frequentes

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.

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Dispositivos Relacionados (Código: MAX)

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Fonte oficial

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