NuVasive AttraX Scaffold— 510(k) K172497
Substantially EquivalentNu Vasive, Incorporated
FDA 510(k) clearance K172497 for NuVasive AttraX Scaffold, Substantially Equivalent on 2017-11-24. Applicant: Nu Vasive, Incorporated. Device class: 2.
Clearance details
- Applicant
- Nu Vasive, Incorporated
- Product code
- Code MQV
- Device class
- Class 2
- Regulation
- 21 CFR 888.3045
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Diego, CA, US
Recent devices under product code MQV
view allMore clearances from Nu Vasive, Incorporated
view allAdverse events under product code MQV
product code MQV- Death
- 6
- Injury
- 435
- Total
- 441
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.