Atlas FDA

Concerto Versa, Detachable Coil

FDA 510(k) clearance K202850 · decided 2021-02-09

Clearance details

K-number
K202850
Device name
Concerto Versa, Detachable Coil
Applicant
Micro Therapeutics, Inc. d/b/a ev3 Neurovascular
Decision
Substantially Equivalent
Date received
2020-09-28
Decision date
2021-02-09
Days to decision
134 days
Clearance type
Traditional
Product code
KRD
Device class
2
Regulation number
870.3300
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Irvine, CA, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Micro Therapeutics

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
UniPearls® Embolic Microspheres (K252812)Suzhou Haowei Medical Technology Co., Ltd.2026-07-31
OBSIDIO Conformable Embolic (K261488)Boston Scientific Corporation2026-07-24
Concerto Versa™ Detachable Coil (K261866)Medtronic, Inc.2026-06-24
HARBOR Occlusion Device (K260635)Nuvascular, Inc.2026-06-12
LOBO Vascular Occlusion System (K260508)Okami Medical, Inc.2026-04-10
Concerto Versa™ Detachable Coil (K253511)Medtronic, Inc.2026-01-14
Tembo Embolic System (K253677)Instylla, Inc.2025-12-15
OBSIDIO™ Conformable Embolic (M0013972101010) (K253376)Boston Scientific Corporation2025-10-30
Polyvinyl Alcohol Embolic Microspheres (K250209)Canyon Medical, Inc.2025-09-23
HARBOR Occlusion Device (K250133)Nuvascular, Inc.2025-07-09
Prestige Coil System (Prestige Packing Line Extension) (K251383)Balt USA, LLC2025-05-30
Embosphere Microspheres (K250971)Biosphere Medical, S.A.2025-05-16

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
Pipeline™ Vantage Embolization Device with Shield Technology™ (P100018/S048)Micro Therapeutics, Inc. d/b/a ev3 Neurovascular2025-08-14
Pipeline™ Flex Embolization Device (Pipeline™ Flex); Pipeline™ Flex Embolization Device with Shield Technology™ (Pipelin (P100018/S051)Micro Therapeutics, Inc. d/b/a ev3 Neurovascular2025-06-04
Pipeline Flex Embolization Device; Pipeline Flex Embolization Device with Shield Technology (Pipeline™ Shield) (P100018/S050)Micro Therapeutics, Inc. d/b/a ev3 Neurovascular2025-03-27
Pipeline™ Vantage Embolization Device with Shield Technology™ (Pipeline™ Vantage) (P100018/S049)Micro Therapeutics, Inc. d/b/a ev3 Neurovascular2025-03-05
Pipeline™ Flex Embolization Device with Shield Technology™, Pipeline™ Vantage Embolization Device with Shield Technology (P100018/S047)Micro Therapeutics, Inc. d/b/a ev3 Neurovascular2024-09-20
Pipeline™ Flex Embolization Device with Shield Technology™, Pipeline™ Vantage Embolization Device with Shield Technology (P100018/S046)Micro Therapeutics, Inc. d/b/a ev3 Neurovascular2024-07-26
Pipeline™ Vantage Embolization Device with Shield Technology™ (P100018/S043)Micro Therapeutics, Inc. d/b/a ev3 Neurovascular2024-06-06
Pipeline™ Flex Embolization Device with Shield Technology™ (PED2), Pipeline™ Vantage Embolization Device with Shield Tec (P100018/S044)Micro Therapeutics, Inc. d/b/a ev3 Neurovascular2024-04-25