Cleared Traditional

K864018 - HACKSAW
(FDA 510(k) Clearance)

K864018 · Med-Tool, Inc. · General & Plastic Surgery
Oct 1986
Decision
15d
Days
Risk

K864018 is an FDA 510(k) clearance for the HACKSAW..

Submitted by Med-Tool, Inc. (St. Louis, US). The FDA issued a Cleared decision on October 30, 1986, 15 days after receiving the submission on October 15, 1986.

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

Submission Details

510(k) Number K864018 FDA.gov
FDA Decision Cleared SESE
Date Received October 15, 1986
Decision Date October 30, 1986
Days to Decision 15 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary

Device Classification

Product Code
Device Class