FDA 510(k)

TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System

K-Nummer: K251502 · 2025-07-07

Entscheidungsdatum2025-07-07

ProduktcodeMAX

BeratungsausschussOR

EntscheidungSubstantially Equivalent

Produktübersicht

TruLift® Lateral Expandable Spacer & Lateral Buttress Plate 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 2025-07-07 under 510(k) number K251502. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Häufig gestellte Fragen

What is the TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System?

TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System is a medical device that received FDA 510(k) clearance on 2025-07-07. The listed applicant is Life Spine, Inc.. The 510(k) number is K251502.

When did TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System receive FDA 510(k) clearance?

TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System received FDA 510(k) clearance on 2025-07-07, under 510(k) number K251502.

Who is the listed applicant for TruLift® Lateral Expandable Spacer & Lateral Buttress Plate 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 TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System?

The FDA product code for TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System is MAX.

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Weitere Einträge mit Life Spine, Inc. als Antragsteller

K261430TruLift Expandable System K260571SIMPACT Sacroiliac Joint Fixation System GX Navigation Instruments K260837VersaLift Expandable System K254274ARx® SAI Implantatsystem K253748Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer System K250373ProLift Expandable Spacer System

Alle 66 Geräte anzeigen →

Verwandte Geräte (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 SystemSeaSpine Orthopedics Corporation K253151Fule Interbody Fusion Cage SystemBeijing Fule Science & Technology Development Co., Ltd.

Offizielle Quelle

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