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The Tracker / September 2026 / K260677

510(k) cleared

Vessel Closure Device (VCD177213P)

Vcd Medical S.R.L. · Sep 17, 2026 · K260677

FDA cleared the Vessel Closure Device (VCD177213P) from Vcd Medical S.R.L. on Sep 17, 2026 under K260677, a traditional 510(k). The device falls under product code FZP, Clip, Implantable, regulated at 21 CFR 878.4300 as a Class 2 device. The review panel was General, Plastic Surgery.

FDA logged the submission as received on Mar 2, 2026. The decision came 199 days later, longer than the 90 FDA-day review goal, which usually means at least one additional information request.

This is the only decision on file for Vcd Medical S.R.L. in the last 12 months of the tracker.

Questions & Answers

What did FDA clear under K260677?

K260677 is the FDA 510(k) for Vessel Closure Device (VCD177213P), submitted by Vcd Medical S.R.L.. FDA's decision date was Sep 17, 2026, under product code FZP (Clip, Implantable).

Who makes the Vessel Closure Device (VCD177213P)?

Vcd Medical S.R.L., based in Brescia, is the applicant of record for K260677.

How long did the K260677 review take?

FDA received the submission on Mar 2, 2026 and issued its decision on Sep 17, 2026, 199 days later.

← All decisions in September 2026