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. Device class: 2.

Clearance details

Applicant: Mitek Worldwide
Product code: Code NOV
Device class: Class 2
Regulation: 21 CFR 888.3030
Advisory panel: Orthopedic
Date received: 2003-07-07
Decision date: 2003-08-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norwood, MA, US

Download summary PDF View on FDA.gov ↗

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K030995 — MINILOK QUICKANCHOR PLUS2003-06-26
K031519 — CUFFLOK ANCHOR2003-06-06
K031406 — EXOJET TISSUE MANAGEMENT SYSTEM2003-05-30

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