GII QUICKANCHOR PLUS WITH ORTHOCORD SUTURE— 510(k) K051989
Substantially EquivalentDepuy Mitek, A Johnson & Johnson Company
FDA 510(k) clearance K051989 for GII QUICKANCHOR PLUS WITH ORTHOCORD SUTURE, Substantially Equivalent on 2005-08-05. Applicant: Depuy Mitek, A Johnson & Johnson Company.
Clearance details
- Applicant
- Depuy Mitek, A Johnson & Johnson Company
- Product code
- Code JDR
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Norwood, MA, US
Adverse events under product code JDR
product code JDR- Injury
- 726
- Malfunction
- 663
- Other
- 1
- Total
- 1,390
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.