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FDA 510(k)

SPINAL SPHERE SYSTEM

K-Number: K073274 · 2008-03-17

ApplicantLife Spine
Decision Date2008-03-17
Product CodeNVR
DecisionUnknown

Device Summary

SPINAL SPHERE 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 2008-03-17 under 510(k) number K073274. The device is classified under product code NVR. FDA Decision: Unknown.

Frequently Asked Questions

What is the SPINAL SPHERE SYSTEM?

SPINAL SPHERE SYSTEM is a medical device that received FDA 510(k) clearance on 2008-03-17. The listed applicant is Life Spine. The 510(k) number is K073274.

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

SPINAL SPHERE SYSTEM received FDA 510(k) clearance on 2008-03-17, under 510(k) number K073274.

Who is the listed applicant for SPINAL SPHERE 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 SPINAL SPHERE SYSTEM?

The FDA product code for SPINAL SPHERE SYSTEM is NVR.

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 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

View all 33 devices →

Related Devices (Code: NVR)

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.

K073105PEEK SPINAL SPHERESInterbody Innovations, LlpK062992SPINAL SPHERESInterbody Innovations, LlpK063139SPINAL STABILIZING SPHERE SYSTEMBiomet SpineK060415MODIFICATION TO: SATELLITE SPINAL SYSTEMMedtronic Sofamor DanekK051320SATELLITE SPINAL SYSTEMMedtronic Sofamor Danek

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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