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FDA 510(k)

ALIF SPINAL TRUSS INTERBODY FUSION DEVICE

K-Number: K083894 · 2011-01-18

Decision Date2011-01-18
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ALIF SPINAL TRUSS INTERBODY FUSION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is 4-Web Spine, LLC. It received FDA 510(k) clearance on 2011-01-18 under 510(k) number K083894. 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 ALIF SPINAL TRUSS INTERBODY FUSION DEVICE?

ALIF SPINAL TRUSS INTERBODY FUSION DEVICE is a medical device that received FDA 510(k) clearance on 2011-01-18. The listed applicant is 4-Web Spine, LLC. The 510(k) number is K083894.

When did ALIF SPINAL TRUSS INTERBODY FUSION DEVICE receive FDA 510(k) clearance?

ALIF SPINAL TRUSS INTERBODY FUSION DEVICE received FDA 510(k) clearance on 2011-01-18, under 510(k) number K083894.

Who is the listed applicant for ALIF SPINAL TRUSS INTERBODY FUSION DEVICE?

The FDA 510(k) record lists 4-Web Spine, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALIF SPINAL TRUSS INTERBODY FUSION DEVICE?

The FDA product code for ALIF SPINAL TRUSS INTERBODY FUSION DEVICE is MAX.

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.

Related Devices (Code: MAX)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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