FDA Registration Active 🇺🇸 United States

Flextome Cutting Balloon Microsurgical Dilatation Device

Reg #: 1000121056 · FEI: 1000121056 · Expires 2025
Products
6
Proprietary Names
2
Establishment Types
1
Classifications
6

Registration Details

Registration Name
Boston Scientific Corporation
Registration Number
1000121056
FEI Number
1000121056
Status
Active
Expiry Year
2025
Initial Importer
No
Address
8 Industrial Dr
City
Coventry
State
RI
ZIP
02816
Country
US

Regulatory Submissions

PMA Number
P950020

Owner / Operator

Firm Name
Boston Scientific Corporation
Operator Number
9912058
Address
300 Boston Scientific Way
City
Marlborough
State
MA
Postal Code
01752
Country
US

Products

Device Name Product Code
Catheters, Transluminal Coronary Angioplasty, Percutaneous LOX
Stent, Renal NIN
Catheter, Percutaneous Transluminal Coronary Angioplasty (Ptca), Cutting/Scoring NWX
Coronary Drug-Eluting Stent NIQ
Stent, Coronary MAF
Catheter, Angioplasty, Peripheral, Transluminal LIT

Proprietary Names

Flextome Cutting Balloon Microsurgical Dilatation Device Wolverine Coronary Cutting Balloon Microsurgical Dilatation Device

Establishment Types

Manufacture Medical Device