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FDA 510(k)

VUSION TS, PS, AND CS PARTIAL VERTEBRAL BODY REPLACEMENTS

K-Number: K062666 · 2007-01-25

ApplicantOrtho Development Corp.
Decision Date2007-01-25
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VUSION TS, PS, AND CS PARTIAL VERTEBRAL BODY REPLACEMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Ortho Development Corp.. It received FDA 510(k) clearance on 2007-01-25 under 510(k) number K062666. The device is classified under product code MQP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VUSION TS, PS, AND CS PARTIAL VERTEBRAL BODY REPLACEMENTS?

VUSION TS, PS, AND CS PARTIAL VERTEBRAL BODY REPLACEMENTS is a medical device that received FDA 510(k) clearance on 2007-01-25. The listed applicant is Ortho Development Corp.. The 510(k) number is K062666.

When did VUSION TS, PS, AND CS PARTIAL VERTEBRAL BODY REPLACEMENTS receive FDA 510(k) clearance?

VUSION TS, PS, AND CS PARTIAL VERTEBRAL BODY REPLACEMENTS received FDA 510(k) clearance on 2007-01-25, under 510(k) number K062666.

Who is the listed applicant for VUSION TS, PS, AND CS PARTIAL VERTEBRAL BODY REPLACEMENTS?

The FDA 510(k) record lists Ortho Development Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VUSION TS, PS, AND CS PARTIAL VERTEBRAL BODY REPLACEMENTS?

The FDA product code for VUSION TS, PS, AND CS PARTIAL VERTEBRAL BODY REPLACEMENTS is MQP.

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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.

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