MITEK MICRO QUICKANCHOR— 510(k) K032078
Substantially EquivalentMitek Worldwide
FDA 510(k) clearance K032078 for MITEK MICRO QUICKANCHOR, Substantially Equivalent on 2003-08-25. Applicant: Mitek Worldwide.
Clearance details
- Applicant
- Mitek Worldwide
- Product code
- Code NOV
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Norwood, MA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.