MITEK MINI ANCHOR— 510(k) K936311

Name: FDA 510(k) clearance K936311
Creator: U.S. Food and Drug Administration
Published: 1995-10-31

Substantially Equivalent for Some Indications

Mitek Surgical Products, Inc.

FDA 510(k) clearance K936311 for MITEK MINI ANCHOR, Substantially Equivalent for Some Indications on 1995-10-31. Applicant: Mitek Surgical Products, Inc.. Device class: 2.

Clearance details

Applicant: Mitek Surgical Products, Inc.
Product code: Code MNV
Device class: Class 2
Regulation: 21 CFR 876.5820
Advisory panel: Gastroenterology, Urology
Date received: 1994-04-20
Decision date: 1995-10-31
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Norwood, MA, US

Download summary PDF View on FDA.gov ↗

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