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FDA 510(k)

ProLift® Expandable System

K-Number: K173182 · 2017-12-20

ApplicantLife Spine, Inc.
Decision Date2017-12-20
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ProLift® Expandable 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 2017-12-20 under 510(k) number K173182. 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® Expandable System?

ProLift® Expandable System is a medical device that received FDA 510(k) clearance on 2017-12-20. The listed applicant is Life Spine, Inc.. The 510(k) number is K173182.

When did ProLift® Expandable System receive FDA 510(k) clearance?

ProLift® Expandable System received FDA 510(k) clearance on 2017-12-20, under 510(k) number K173182.

Who is the listed applicant for ProLift® Expandable 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 ProLift® Expandable System?

The FDA product code for ProLift® Expandable System is MAX.

Other records listing Life Spine, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261430TruLift Expandable SystemK260571SIMPACT Sacroiliac Joint Fixation System GX Navigation InstrumentsK260837VersaLift Expandable SystemK254274ARx® SAI Implant SystemK253748Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer SystemK251502TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System

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Related Devices (Code: MAX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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 CorporationK253151Fule Interbody Fusion Cage SystemBeijing Fule Science & Technology Development Co., Ltd.K261159Exceed® Biplanar Expandable Interbody SystemSpine Wave, 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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