Concerto Versa™ Detachable Coil
K-Number: K261866 · 2026-06-24
Device Summary
Frequently Asked Questions
What is the Concerto Versa™ Detachable Coil?
Concerto Versa™ Detachable Coil is a medical device that received FDA 510(k) clearance on 2026-06-24. The listed applicant is Medtronic, Inc.. The 510(k) number is K261866.
When did Concerto Versa™ Detachable Coil receive FDA 510(k) clearance?
Concerto Versa™ Detachable Coil received FDA 510(k) clearance on 2026-06-24, under 510(k) number K261866.
Who is the listed applicant for Concerto Versa™ Detachable Coil?
The FDA 510(k) record lists Medtronic, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Concerto Versa™ Detachable Coil?
The FDA product code for Concerto Versa™ Detachable Coil is KRD.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Medtronic, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: KRD)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.