Skyway Anterior Cervical Plate System— 510(k) K250486
Substantially EquivalentKyocera Medical Technologies Inc. (KMTI)
FDA 510(k) clearance K250486 for Skyway Anterior Cervical Plate System, Substantially Equivalent on 2025-04-10. Applicant: Kyocera Medical Technologies Inc. (KMTI).
Clearance details
- Applicant
- Kyocera Medical Technologies Inc. (KMTI)
- Product code
- Code KWQ
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Redlands, CA, US
Adverse events under product code KWQ
product code KWQ- Death
- 8
- Injury
- 1,212
- Malfunction
- 1,233
- Total
- 2,453
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.