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FDA 510(k)

SpineView X-Pac Expandable Lumbar Cage System

K-Number: K160856 · 2016-08-01

Decision Date2016-08-01
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SpineView X-Pac Expandable Lumbar Cage System is a medical device manufactured by Spine View, Inc.. It received FDA 510(k) clearance on 2016-08-01 under approval number K160856. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SpineView X-Pac Expandable Lumbar Cage System?

SpineView X-Pac Expandable Lumbar Cage System is a medical device that received FDA 510(k) clearance on 2016-08-01. It is manufactured by Spine View, Inc.. The 510(k) number is K160856.

When was SpineView X-Pac Expandable Lumbar Cage System approved by the FDA?

SpineView X-Pac Expandable Lumbar Cage System received FDA 510(k) clearance on 2016-08-01, under approval number K160856.

What company makes SpineView X-Pac Expandable Lumbar Cage System?

SpineView X-Pac Expandable Lumbar Cage System is manufactured by Spine View, Inc..

What is the FDA product code for SpineView X-Pac Expandable Lumbar Cage System?

The FDA product code for SpineView X-Pac Expandable Lumbar Cage System is MAX.

Related Clinical Trials

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Official Source

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