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FDA 510(k)

Solidity Vertebral Body Replacement

K-Number: K181921 · 2018-11-16

ApplicantUlrich Medical USA
Decision Date2018-11-16
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Solidity Vertebral Body Replacement is a medical device manufactured by Ulrich Medical USA. It received FDA 510(k) clearance on 2018-11-16 under approval number K181921. 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 Solidity Vertebral Body Replacement?

Solidity Vertebral Body Replacement is a medical device that received FDA 510(k) clearance on 2018-11-16. It is manufactured by Ulrich Medical USA. The 510(k) number is K181921.

When was Solidity Vertebral Body Replacement approved by the FDA?

Solidity Vertebral Body Replacement received FDA 510(k) clearance on 2018-11-16, under approval number K181921.

What company makes Solidity Vertebral Body Replacement?

Solidity Vertebral Body Replacement is manufactured by Ulrich Medical USA.

What is the FDA product code for Solidity Vertebral Body Replacement?

The FDA product code for Solidity Vertebral Body Replacement 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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