Ortho Pared Instruments, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K831772 | GUILLOTINE BLADE | July 7, 1983 |
| K820225 | MENISCUS EXTRACTOR | February 4, 1982 |
| K820226 | UNIVERSALL DRILL GUIDE | February 4, 1982 |
| K812566 | UNIVERSAL SUTURE PASSER | November 10, 1981 |