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FDA 510(k)

SPINEFRONTIER DORADO VBR

K-Number: K072289 · 2007-11-01

ApplicantSpinefrontier, Inc.
Decision Date2007-11-01
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SPINEFRONTIER DORADO VBR is the device name listed in this FDA 510(k) record. The listed applicant is Spinefrontier, Inc.. It received FDA 510(k) clearance on 2007-11-01 under 510(k) number K072289. 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 SPINEFRONTIER DORADO VBR?

SPINEFRONTIER DORADO VBR is a medical device that received FDA 510(k) clearance on 2007-11-01. The listed applicant is Spinefrontier, Inc.. The 510(k) number is K072289.

When did SPINEFRONTIER DORADO VBR receive FDA 510(k) clearance?

SPINEFRONTIER DORADO VBR received FDA 510(k) clearance on 2007-11-01, under 510(k) number K072289.

Who is the listed applicant for SPINEFRONTIER DORADO VBR?

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

What is the FDA product code for SPINEFRONTIER DORADO VBR?

The FDA product code for SPINEFRONTIER DORADO VBR is MAX.

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Other records listing Spinefrontier, 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.

K193106SpineFrontier Lumbar Interbody Fusion Device SystemK172484A-CIFT SoloFuseK132740SPINEFRONTIER LESPLASTY POSTERIOR CERVICAL LAMINOPLASTY SYSTEMK123164SPINEFRONTIER PEDFUSE PEDICLE SCREW SYSTEMK121060SPINE FRONTIER INDUS ACP SYSTEMK113518ARENA-C CERVICAL INTERVERTEBRAL BODY FUSION 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.

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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