Phoenix Bioengineering, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K930125 | PHOENIX BONE SCREWS PBS-TYPE SERIES | December 30, 1993 |
| K913490 | PHOENIX BURR HOLE BUTTON, BURR 1 | January 13, 1992 |
| K904434 | SEXTON CYSTOTOMY URINE PUMP (SCUP2) | February 1, 1991 |