HEALIX TI ANCHOR— 510(k) K082282
Substantially EquivalentDepuy Mitek, A Johnson & Johnson Co.
FDA 510(k) clearance K082282 for HEALIX TI ANCHOR, Substantially Equivalent on 2008-11-07. Applicant: Depuy Mitek, A Johnson & Johnson Co..
Clearance details
- Applicant
- Depuy Mitek, A Johnson & Johnson Co.
- Product code
- Code HWC
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Raynham, MA, US
Adverse events under product code HWC
product code HWC- Death
- 20
- Injury
- 15,910
- Malfunction
- 8,192
- Other
- 1
- Total
- 24,123
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.