Advanced Med/Surg, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 10
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K942108 | COHORT BONE BRUSH | October 11, 1994 |
| K931538 | AMSET(TM) CANNULATED BONE SCREW | May 4, 1994 |
| K921642 | AMSEN DOUBLE-ENDED FORAMINAL PROBE | June 3, 1992 |
| K921643 | AMSEN POSTERIOR DISC EVACUATOR | June 3, 1992 |
| K921644 | AMSEN HOCKEY STICK CHISEL | June 3, 1992 |
| K921645 | AMSEN SPINE IMPACTOR INSTRUMENTS | June 3, 1992 |
| K905023 | AMSET LOCKING PLATE SYSTEM | January 31, 1992 |
| K911768 | AMSET(TM) BONE SCREW | October 4, 1991 |
| K905014 | AMSET PLD SYSTEM | April 1, 1991 |
| K903808 | AMSIS RDS, RADIOGRAPHIC DISCOGRAPHY KIT | January 22, 1991 |