FDA 510(k)

INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE

K-Number: K080673 · 2008-06-10

Decision Date2008-06-10

Product CodeMAX

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Vertebral Technologies, Inc.. It received FDA 510(k) clearance on 2008-06-10 under 510(k) number K080673. 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 INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE?

INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE is a medical device that received FDA 510(k) clearance on 2008-06-10. The listed applicant is Vertebral Technologies, Inc.. The 510(k) number is K080673.

When did INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE receive FDA 510(k) clearance?

INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE received FDA 510(k) clearance on 2008-06-10, under 510(k) number K080673.

Who is the listed applicant for INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE?

The FDA 510(k) record lists Vertebral Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE?

The FDA product code for INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE is MAX.

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Other records listing Vertebral Technologies, Inc. as applicant

K131540INTERFUSE L INTERVERTEBRAL BODY FUSION DEVICE K110226INTERFUSE T INVERTEBRAL BODY FUSION DEVICE K110045INTERFUSE DA INVERTEBRAL BODY FUSION DEVICE K102277INTERFUSE T INVERTEBRAL BODY FUSION DEVICE K093675INTERFUSE INVERTEBRAL BODY FUSION DEVICE MODEL 9076 K091988MODIFICATION TO: INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE , MODEL 9076

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Related Devices (Code: MAX)

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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.