MITEK MICRO QUICKANCHOR— 510(k) K032078

Substantially Equivalent

Mitek 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
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Data sourced from openFDA. This site is unofficial and independent of the FDA.