NuVasive AttraX Scaffold— 510(k) K240507
Substantially EquivalentNuvasive, Inc.
FDA 510(k) clearance K240507 for NuVasive AttraX Scaffold, Substantially Equivalent on 2024-03-20. Applicant: Nuvasive, Inc.. Device class: 2.
Clearance details
- Applicant
- Nuvasive, Inc.
- 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
- Special
- Location
- San Diego, CA, US
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More clearances from Nuvasive, Inc.
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.