FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Drug Coated Prostatic Dilation Catheter For Benign Prostatic Hyperplasia
PMA: P220029
·
Supplement: S001
·
Decision Aug 25, 2023
Classifications
1
FEI Numbers
2
Registration Numbers
2
Basic Information
- Device Name
- Drug Coated Prostatic Dilation Catheter For Benign Prostatic Hyperplasia
- Trade Name
- Optilume BPH Catheter System
- PMA Number
- P220029
- Supplement Number
- S001
- Device Class
- FDA Class 3
- Product Code
- QXB
- Generic Name
- Drug coated prostatic dilation catheter for benign prostatic hyperplasia
- Medical Specialty
- Unknown
- Advisory Committee
- Gastroenterology, Urology
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- August 25, 2023
- Date Received
- July 27, 2023
- Supplement Type
- Normal 180 Day Track No User Fee
- Supplement Reason
- Postapproval Study Protocol
- Expedited Review
- N
Advisory Committee Statement
Approval of the protocol for the post-approval study (PAS) protocol.
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| QXB | Drug Coated Prostatic Dilation Catheter For Benign Prostatic Hyperplasia | FDA class 3 | Unknown |