PathLoc-L MIS Spinal System— 510(k) K183117
Substantially EquivalentL&K BIOMED Co., Ltd.
FDA 510(k) clearance K183117 for PathLoc-L MIS Spinal System, Substantially Equivalent on 2018-11-15. Applicant: L&K BIOMED Co., Ltd..
Clearance details
- Applicant
- L&K BIOMED Co., Ltd.
- Product code
- Code NKB
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Yongin-Si, KR
Adverse events under product code NKB
product code NKB- Death
- 27
- Injury
- 5,033
- Malfunction
- 4,140
- Total
- 9,200
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.