FDA 510(k)

UNiD Patient-matched PLIF cage

K-Number: K182158 · 2019-07-15

Decision Date2019-07-15

Product CodeMAX

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

UNiD Patient-matched PLIF cage is a medical device manufactured by Medicrea International SA. It received FDA 510(k) clearance on 2019-07-15 under approval number K182158. 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 UNiD Patient-matched PLIF cage?

UNiD Patient-matched PLIF cage is a medical device that received FDA 510(k) clearance on 2019-07-15. It is manufactured by Medicrea International SA. The 510(k) number is K182158.

When was UNiD Patient-matched PLIF cage approved by the FDA?

UNiD Patient-matched PLIF cage received FDA 510(k) clearance on 2019-07-15, under approval number K182158.

What company makes UNiD Patient-matched PLIF cage?

UNiD Patient-matched PLIF cage is manufactured by Medicrea International SA.

What is the FDA product code for UNiD Patient-matched PLIF cage?

The FDA product code for UNiD Patient-matched PLIF cage is 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.