Scholten Surgical Instruments, Inc.
Scholten Surgical Instruments, Inc. appears in FDA public data with 0 recalls, 8 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 3, 2007.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K072051 | NOVATOME, MODEL: SU101-50 | October 3, 2007 |
| K900405 | SCHOLTEN FRAME | March 1, 1990 |
| K852331 | SYS, ANGIOGRAPHIC, SINGLE-OR BI-PLANE RADIOGRAPHIC | August 1, 1986 |
| K852119 | TEMPORARY PACEMAKER GROUND WIRE | September 15, 1985 |
| K852120 | FORCEPS, BIOPSY(NON RIGID) | July 2, 1985 |
| K852332 | TABLE ACCESSORIES, OPERATING ROOM | July 2, 1985 |
| K852330 | RETRACTOR, SURGICAL | June 27, 1985 |
| K852329 | STAND, OPERATING ROOM | June 14, 1985 |