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FDA 510(k)

LIFE SPINE FACET SCREW SPINAL SYSTEM

K-Number: K090865 · 2009-06-26

ApplicantLife Spine
Decision Date2009-06-26
Product CodeMRW
DecisionSubstantially Equivalent

Device Summary

LIFE SPINE FACET SCREW 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 2009-06-26 under 510(k) number K090865. The device is classified under product code MRW. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFE SPINE FACET SCREW SPINAL SYSTEM?

LIFE SPINE FACET SCREW SPINAL SYSTEM is a medical device that received FDA 510(k) clearance on 2009-06-26. The listed applicant is Life Spine. The 510(k) number is K090865.

When did LIFE SPINE FACET SCREW SPINAL SYSTEM receive FDA 510(k) clearance?

LIFE SPINE FACET SCREW SPINAL SYSTEM received FDA 510(k) clearance on 2009-06-26, under 510(k) number K090865.

Who is the listed applicant for LIFE SPINE FACET SCREW 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 LIFE SPINE FACET SCREW SPINAL SYSTEM?

The FDA product code for LIFE SPINE FACET SCREW SPINAL SYSTEM is MRW.

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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: MRW)

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.

K262618Arthrex Spine Compression FT ScrewArthrex, Inc.K261209Ion-LSurGenTec, LLCK253676CORUS™ Posterior Cervical Stabilization System 3D (CORUS™ PCSS 3D)Providence Medical Technology, Inc.K253432DiversiVy™ Facet Screw SystemVy Spine, LLCK251714Ion-CSurGenTec, LLCK250679FFX Facet Fixation SystemSc Medica

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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