Durasphere® Injectable Bulking Agent
FDA premarket approval P980053/S020 · decided 2024-01-18
Approval details
- PMA number
- P980053
- Supplement
- S020
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Durasphere® Injectable Bulking Agent
- Generic name
- AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE
- Applicant
- Carbon Medical Technologies, Inc.
- Date received
- 2023-12-18
- Decision date
- 2024-01-18
- Days to decision
- 31 days
- Decision code
- OK30
- Product code
- LNM
- Advisory committee
- Gastroenterology, Urology
- Expedited review
- No
- Location
- St. Paul, MN
- Statement
- changes to the sterilization parameters
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
| Record | Firm | Date |
|---|---|---|
| InjecSURE Injection System (K253598) | Carbon Medical Technologies, Inc. | 2026-03-31 |
| MammoSTAR Biopsy Site Identifier (K251748) | Carbon Medical Technologies, Inc. | 2025-07-23 |
| Fiducial Marker (K211590) | Carbon Medical Technologies, Inc. | 2021-06-10 |
| Endoscopic Injection Needle (K172227) | Carbon Medical Technologies, Inc. | 2017-08-23 |
| BIOMARC COAXIAL NEEDLE (K133148) | Carbon Medical Technologies, Inc. | 2014-05-13 |
| BIOMARC FIDUCIAL MARKER (K132064) | Carbon Medical Technologies, Inc. | 2014-02-28 |
| BIOMARC FIDUCIAL MARKER (K132708) | Carbon Medical Technologies, Inc. | 2013-12-20 |
| BIOMARC GOLD FIDUCIAL MARKER (K130678) | Carbon Medical Technologies, Inc. | 2013-04-12 |