Cleared Traditional

MATRIX DRI-IDEA BOOTIES

K850661 · Matrix Medica, Inc. · General & Plastic Surgery

Mar 1985

Decision

19d

Days

—

Risk

About This 510(k) Submission

K850661 is an FDA 510(k) clearance for the MATRIX DRI-IDEA BOOTIES, submitted by Matrix Medica, Inc. (Minden, US). The FDA issued a Cleared decision on March 11, 1985, 19 days after receiving the submission on February 20, 1985. This device falls under the General & Plastic Surgery review panel.

Submission Details

510(k) Number	K850661 FDA.gov
FDA Decision	Cleared SESE
Date Received	February 20, 1985
Decision Date	March 11, 1985
Days to Decision	19 days
Submission Type	Traditional
Review Panel	General & Plastic Surgery (SU)
Summary	—