Protégé EverFlex Self-expanding Peripheral Stent System
Medtronic, Inc. · Gastroenterology, Urology
Open FDA's page for this record- Third party flag
- N
- City
- Plymouth
- Advisory committee description
- Gastroenterology, Urology
- Address 1
- 2300 Berkshire Ln. N.
- Statement or summary
- Summary
- Product code
- FGE
- Zip code
- 55441
- Applicant
- Medtronic, Inc.
- Decision date
- 2026-09-17
- Decision code
- SESE
- Country code
- US
- Device name
- Protégé EverFlex Self-expanding Peripheral Stent System
- Advisory committee
- GU
- Contact
- Kim Wallner
- K number
- K262913
- State
- MN
- Date received
- 2026-08-19
- Review advisory committee
- GU
- Postal code
- 55441
- Decision description
- Substantially Equivalent
- Clearance type
- Special
- Harmonized identifiers (openFDA)
- Device name
- Stents, Drains And Dilators For The Biliary Ducts
- Medical specialty description
- Gastroenterology, Urology
- Regulation number
- 876.5010
- Device class
- 2
- Registration number
- 3004129994, 3012480535, 9681442, 3021009035, 3013247477, 3013162291, 3005580113, 3021632375, 3009906660, 3010220595, 1000121056, 3007146453, 3004111573, 1644312, 3014222368, 2126666, 1820334, 3005089785, 3009526575, 3030733800, 1643817, 3010288205, 3031276312, 2020394, 1223925, 9710284, 3015309643, 2134265, 3041276591, 1317547, 2032098, 3008492676, 3030446844, 1319211, 3008146331, 1123137, 9680794, 1531050, 1018233, 3005941719 +107 more
- FEI number
- 3004129994, 3003528016, 3012480535, 3021009035, 3013247477, 3013162291, 3005580113, 3021632375, 3009906660, 3003995201, 3010220595, 1000121056, 3007146453, 3004111573, 2126666, 3014222368, 1820334, 3005089785, 3003565456, 3003084171, 3009526575, 1000123180, 3030733800, 1643817, 3010288205, 3031276312, 2020394, 3015309643, 3041276591, 1317547, 3002807439, 1000122656, 3008492676, 3030446844, 1319211, 3008146331, 3002806565, 1000512168, 1018233, 3002755653 +107 more
