Cleared Traditional

K851896 - DOUBLE ACTION PIN CUTTER
(FDA 510(k) Clearance)

K851896 · Med-Tool, Inc. · General & Plastic Surgery device
May 1985
Decision
21d
Days
—
Risk

K851896 is an FDA 510(k) clearance for the DOUBLE ACTION PIN CUTTER..

Submitted by Med-Tool, Inc. (St. Louis, US). The FDA issued a Cleared decision on May 21, 1985, 21 days after receiving the submission on April 30, 1985.

This device falls under the General & Plastic Surgery FDA review panel.

Submission Details

510(k) Number K851896 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 30, 1985
Decision Date May 21, 1985
Days to Decision 21 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary —

Device Classification

Product Code —
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