QUICKANCHOR (TM)— 510(k) K904436

Substantially Equivalent

Mitek Surgical Products, Inc.

FDA 510(k) clearance K904436 for QUICKANCHOR (TM), Substantially Equivalent on 1990-12-11. Applicant: Mitek Surgical Products, Inc.. Device class: 2.

Clearance details

Applicant: Mitek Surgical Products, Inc.
Product code: Code GAS
Device class: Class 2
Regulation: 21 CFR 878.5000
Advisory panel: General, Plastic Surgery
Date received: 1990-09-28
Decision date: 1990-12-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norwood, MA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Mitek Surgical Products, Inc.

K953560 — MITEK THREADED ANCHOR (FASTIN)1996-01-31
K953877 — MITEK GII ANCHOR1995-12-29
K936311 — MITEK MINI ANCHOR1995-10-31
K941599 — MITEK ABSORBABLE ANCHOR1995-10-24
K944051 — ABSORBALBE ANCHOR1995-08-02

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