Vertebral Technologies, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 7
- Inspections
- 4
- Compliance Actions
- 1
Recent Recalls
| Number | Class | Product | Date |
|---|
| Z-1151-2017 | Class II | InterFuse Tail Traction Tool, Part Number 9116. The InterFuse Tail Traction Tool is an optional Cla | January 13, 2017 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K131540 | INTERFUSE L INTERVERTEBRAL BODY FUSION DEVICE | September 3, 2013 |
| K110226 | INTERFUSE T INVERTEBRAL BODY FUSION DEVICE | May 27, 2011 |
| K110045 | INTERFUSE DA INVERTEBRAL BODY FUSION DEVICE | February 3, 2011 |
| K102277 | INTERFUSE T INVERTEBRAL BODY FUSION DEVICE | October 6, 2010 |
| K093675 | INTERFUSE INVERTEBRAL BODY FUSION DEVICE MODEL 9076 | December 23, 2009 |
| K091988 | MODIFICATION TO: INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE , MODEL 9076 | July 30, 2009 |
| K080673 | INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE | June 10, 2008 |