FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Concerto Versa™ Detachable Coil

K Number: K253511 · Decision Jan 14, 2026
Classifications
1
FEI Numbers
103
Registration Numbers
103
Same Product Code
128
Applicant Total
209
Review Days
70

Basic Information

Device Name
Concerto Versa™ Detachable Coil
K Number
K253511
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.3300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtronic, Inc.
Date Received
November 5, 2025
Decision Date
January 14, 2026
Product Code
KRD
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KRD Device, Vascular, For Promoting Embolization

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KRD), ordered by most recent decision date.

View all

Other Clearances by Medtronic, Inc.

K Number Device Name
K260195 Elongated One-Piece Arterial (EOPA) 3D™ Arterial Cannulae
K253203 Retrograde Coronary Sinus Perfusion Cannulae
K253998 Clearview Intracoronary Shunts
K251831 Bio-Medicus Life Support Catheter and Introducer
K253409 C320LBB Delivery System (C320LBBS45), C320LBB Delivery System (C320LBBS48), C320LBB Delivery System (C320LBBL45), C320LBB Delivery System (C320LBBL48)
K251258 MC2™ Two-Stage Venous Cannula; MC2X™ Three-Stage Venous Cannula
K250075 Medtronic Stedi Extra Support Guidewire
K250199 VitalFlow Console
K250558 SelectSite C304 Deflectable Catheter System (C304); C315 Delivery System (C315)
K242705 Streamline Unipolar Pediatric Temporary Pacing Lead (6491) Streamline Unipolar Temporary Atrial Pacing Lead (6492) Streamline Unipolar Temporary Myocardial Pacing Wire (6494) Streamline Bipolar Temporary Myocardial Pacing Lead (6495) Streamline Unipolar Temporary Myocardial Pacing Lead (6500)
Search all 209 clearances from Medtronic, Inc. →