FDA 510(k)

Trilor Disks, Blocks and Arches

K-Number: K173643 · 2018-02-24

Decision Date2018-02-24

Product CodeEBF

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

Trilor Disks, Blocks and Arches is a medical device manufactured by Bioloren S.R.L.. It received FDA 510(k) clearance on 2018-02-24 under approval number K173643. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Trilor Disks, Blocks and Arches?

Trilor Disks, Blocks and Arches is a medical device that received FDA 510(k) clearance on 2018-02-24. It is manufactured by Bioloren S.R.L.. The 510(k) number is K173643.

When was Trilor Disks, Blocks and Arches approved by the FDA?

Trilor Disks, Blocks and Arches received FDA 510(k) clearance on 2018-02-24, under approval number K173643.

What company makes Trilor Disks, Blocks and Arches?

Trilor Disks, Blocks and Arches is manufactured by Bioloren S.R.L..

What is the FDA product code for Trilor Disks, Blocks and Arches?

The FDA product code for Trilor Disks, Blocks and Arches is EBF.

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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.