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FDA 510(k)

CONQUEST SPINAL SYSTEM

K-Number: K080767 · 2008-05-21

ApplicantLife Spine
Decision Date2008-05-21
Product CodeMNI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CONQUEST SPINAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Life Spine. It received FDA 510(k) clearance on 2008-05-21 under 510(k) number K080767. The device is classified under product code MNI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONQUEST SPINAL SYSTEM?

CONQUEST SPINAL SYSTEM is a medical device that received FDA 510(k) clearance on 2008-05-21. The listed applicant is Life Spine. The 510(k) number is K080767.

When did CONQUEST SPINAL SYSTEM receive FDA 510(k) clearance?

CONQUEST SPINAL SYSTEM received FDA 510(k) clearance on 2008-05-21, under 510(k) number K080767.

Who is the listed applicant for CONQUEST SPINAL SYSTEM?

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

What is the FDA product code for CONQUEST SPINAL SYSTEM?

The FDA product code for CONQUEST SPINAL SYSTEM is MNI.

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Other records listing Life Spine 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.

K182470Plateau Spacer SystemK160169The Life Spine Subtalar Implant SystemK131077LIFE SPINE PLATEAU SPACER SYSTEMK123373NAUTILUS SPINAL SYSTEMK120998SOLSTICE CROSS CONNECTORK111953NAUTILUS SPINAL SYSTEM

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Related Devices (Code: MNI)

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.

K171497Mikron Spinal Fixation SystemMikron Makina Sanayi Ticaret Co. , Ltd.K160731LumFix Spinal Fixation SytemCG Bio Co., Ltd.K151458Double Medical Universal Spine SystemDouble Medical Technology, Inc.K153273MySpine Pedicle Screw Placement Guides - LPMedacta International S.A.K160124LUMIS Cannulated Pedicle Screw Fixation System, U.L.I.S. Pedicle Screw Fixation SystemSpinevision S.A.K160320PremierShandong Weigao Orthopaedic Device 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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