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FDA 510(k)

LIFE SPINE CROSS CONNECTOR

K-Number: K073480 · 2008-01-04

ApplicantLife Spine
Decision Date2008-01-04
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LIFE SPINE CROSS CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Life Spine. It received FDA 510(k) clearance on 2008-01-04 under 510(k) number K073480. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFE SPINE CROSS CONNECTOR?

LIFE SPINE CROSS CONNECTOR is a medical device that received FDA 510(k) clearance on 2008-01-04. The listed applicant is Life Spine. The 510(k) number is K073480.

When did LIFE SPINE CROSS CONNECTOR receive FDA 510(k) clearance?

LIFE SPINE CROSS CONNECTOR received FDA 510(k) clearance on 2008-01-04, under 510(k) number K073480.

Who is the listed applicant for LIFE SPINE CROSS CONNECTOR?

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 CROSS CONNECTOR?

The FDA product code for LIFE SPINE CROSS CONNECTOR is NKB.

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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: NKB)

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.

K252139Kentrospine Viktr-MIS® Pedicle screw systemRivarp Medical Pvt., Ltd.K262067iFuse Granite Onyx™ Implant SystemSI-BONE, Inc.K262091FRAXION Spinal Fixation SystemOrtler Global Tibbi Gerecler Anonim SirketiK262193RIVA® Posterior Fixation System with NanoACTIV Surface Technology; RIVA® Anchor Sacroiliac Fixation System with NanoACTIV Surface TechnologyXenix MedicalK262828KHEIRON® Spinal Fixation System, including patient specific K-RODS.M.A.I.OK260362QUATTRO Spinal system (Open Configuration); QUATTRO-GADGET Spinal system (MIS Configuration)MANTIZ 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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