Spirus Medical, Inc.
Spirus Medical, Inc. appears in FDA public data with 0 recalls, 5 510(k) clearances, 3 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 6, 2008.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 3
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K080050 | SPIRUS MEDICAL ENDO-EASE ENDOSCOPIC OVERTUBE | May 6, 2008 |
| K080042 | SPIRUS MEDICAL SURGICAL INSTRUMENT | April 3, 2008 |
| K062805 | MODIFICATION TO ENDO-EASE | October 13, 2006 |
| K060235 | ENDO-EASE ENDOSCOPIC OVERTUBE | August 4, 2006 |
| K052084 | ENDO-EASE ENDOSCOPIC OVERTUBE | September 14, 2005 |