Virage OCT Spinal Fixation System— 510(k) K151031
Substantially EquivalentZimmer Spine, Inc.
FDA 510(k) clearance K151031 for Virage OCT Spinal Fixation System, Substantially Equivalent on 2015-06-24. Applicant: Zimmer Spine, Inc..
Clearance details
- Applicant
- Zimmer Spine, Inc.
- Product code
- Code NKG
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Minneapolis, MN, US
Adverse events under product code NKG
product code NKG- Death
- 15
- Injury
- 1,090
- Malfunction
- 529
- Total
- 1,634
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.