DCM Kyphoplasty System— 510(k) K162283
Substantially EquivalentDragon Crown Medical Co., Ltd.
FDA 510(k) clearance K162283 for DCM Kyphoplasty System, Substantially Equivalent on 2017-02-06. Applicant: Dragon Crown Medical Co., Ltd..
Clearance details
- Applicant
- Dragon Crown Medical Co., Ltd.
- Product code
- Code NDN
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Jinan, CN
Adverse events under product code NDN
product code NDN- Death
- 24
- Injury
- 407
- Malfunction
- 1,975
- Total
- 2,406
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.