NuVasive Pulse System— 510(k) K210574
Substantially EquivalentNu Vasive, Incorporated
FDA 510(k) clearance K210574 for NuVasive Pulse System, Substantially Equivalent on 2021-07-29. Applicant: Nu Vasive, Incorporated. Device class: 2.
Clearance details
- Applicant
- Nu Vasive, Incorporated
- Product code
- Code OLO
- Device class
- Class 2
- Regulation
- 21 CFR 882.4560
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Diego, CA, US
Recent devices under product code OLO
view allMore clearances from Nu Vasive, Incorporated
view allAdverse events under product code OLO
product code OLO- Death
- 11
- Injury
- 2,799
- Malfunction
- 11,105
- Other
- 1
- Total
- 13,916
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 →
Recalls naming K210574
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K210574.
Data sourced from openFDA. This site is unofficial and independent of the FDA.