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FDA 510(k)

ALAMO T

K-Number: K120401 · 2012-10-05

ApplicantAlliance Partners, LLC
Decision Date2012-10-05
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ALAMO T is the device name listed in this FDA 510(k) record. The listed applicant is Alliance Partners, LLC. It received FDA 510(k) clearance on 2012-10-05 under 510(k) number K120401. 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 ALAMO T?

ALAMO T is a medical device that received FDA 510(k) clearance on 2012-10-05. The listed applicant is Alliance Partners, LLC. The 510(k) number is K120401.

When did ALAMO T receive FDA 510(k) clearance?

ALAMO T received FDA 510(k) clearance on 2012-10-05, under 510(k) number K120401.

Who is the listed applicant for ALAMO T?

The FDA 510(k) record lists Alliance Partners, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALAMO T?

The FDA product code for ALAMO T is MAX.

Related Clinical Trials

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.

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Other records listing Alliance Partners, LLC 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.

K201521Medina Anterior Cervical Plate SystemK173128Alamo® CK122047ALAMO PK121181SWANNSHIDI BONE MARROW ASPIRATION NEEDLEK112361ALAMO C

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.

K261049SCALA® TLSpineart SAK261430TruLift 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.

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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