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FDA 510(k)

PEEK SPINAL SPHERES

K-Number: K073105 · 2008-01-03

ApplicantInterbody Innovations, Llp
Decision Date2008-01-03
Product CodeNVR
DecisionUnknown

Device Summary

PEEK SPINAL SPHERES is the device name listed in this FDA 510(k) record. The listed applicant is Interbody Innovations, Llp. It received FDA 510(k) clearance on 2008-01-03 under 510(k) number K073105. The device is classified under product code NVR. FDA Decision: Unknown.

Frequently Asked Questions

What is the PEEK SPINAL SPHERES?

PEEK SPINAL SPHERES is a medical device that received FDA 510(k) clearance on 2008-01-03. The listed applicant is Interbody Innovations, Llp. The 510(k) number is K073105.

When did PEEK SPINAL SPHERES receive FDA 510(k) clearance?

PEEK SPINAL SPHERES received FDA 510(k) clearance on 2008-01-03, under 510(k) number K073105.

Who is the listed applicant for PEEK SPINAL SPHERES?

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

What is the FDA product code for PEEK SPINAL SPHERES?

The FDA product code for PEEK SPINAL SPHERES 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 Interbody Innovations, Llp 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.

K081614ZEUS SMALL CERVICAL CAGE AND LARGE, EXTRA LARGE, CURVED AND STRAIGHT LUMBAR CAGESK062992SPINAL SPHERESK051371INTERBODY INNOVATIONS CEMENT RESTRICTOR

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.

K073274SPINAL SPHERE SYSTEMLife SpineK062992SPINAL 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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