Last synced on 9 May 2025 at 11:05 pm

Passeo-35 Xeo Peripheral Dilatation Catheter; Passeo-18 Peripheral Dilatation Catheters; Passeo-14 Peripheral Dilatation Catheter; Oscar Peripheral Multifunctional Catheter System; Pantera Pro Percutaneous Transluminal Coronary Angioplasty Catheter; Pantera LEO Percutaneous Transluminal Coronary Angioplasty (PTCA) Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250706
510(k) Type
Special
Applicant
BIOTRONIK, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/2025
Days to Decision
25 days
Submission Type
Summary

Passeo-35 Xeo Peripheral Dilatation Catheter; Passeo-18 Peripheral Dilatation Catheters; Passeo-14 Peripheral Dilatation Catheter; Oscar Peripheral Multifunctional Catheter System; Pantera Pro Percutaneous Transluminal Coronary Angioplasty Catheter; Pantera LEO Percutaneous Transluminal Coronary Angioplasty (PTCA) Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250706
510(k) Type
Special
Applicant
BIOTRONIK, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/2025
Days to Decision
25 days
Submission Type
Summary