Atlas FDA

Surmodics SurVeil™ Drug-Coated Balloon

FDA premarket approval P210025/S005 · decided 2024-12-20

Approval details

PMA number
P210025
Supplement
S005
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Surmodics SurVeil™ Drug-Coated Balloon
Generic name
Drug-Eluting Peripheral Transluminal Angioplasty Catheter
Applicant
Surmodics,Inc.
Date received
2024-12-02
Decision date
2024-12-20
Days to decision
18 days
Decision code
OK30
Product code
ONU
Advisory committee
Cardiovascular
Expedited review
No
Location
Eden Prairie, MN
Statement
a change to the in-process specification criteria for the balloon base coat solution

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

510(k) clearances by this applicant

RecordFirmDate
Pounce(TM) Sheath (K252227)Surmodics,Inc.2025-09-24
Pounce XL Thrombectomy System (PTS-1011-7F135) (K241362)Surmodics,Inc.2024-09-11
Microcatheter (K232647)Surmodics,Inc.2023-09-29
Pounce™ Sheath (K231828)Surmodics,Inc.2023-09-07
Pounce™ Thrombectomy System (K231022)Surmodics,Inc.2023-06-12
Sublime Microcatheter (K221886)Surmodics,Inc.2022-10-14
Pounce Thrombectomy System (K220501)Surmodics,Inc.2022-03-23
Pounce Thrombectomy System (K211492)Surmodics,Inc.2021-07-30