FDA 510(k) Applications Submitted by Sharon McDermott

FDA 510(k) Number Submission Date Device Name Applicant
K170170 01/19/2017 Valleylab FT10 Electrosurgical Platform Covidien llc
K090348 02/11/2009 CODMAN BACTISEAL EVD CATHETER SET, CODMAN BACTISEAL CLEAR EVD CATHETER SET Codman & Shurtleff, Inc.
K160539 02/26/2016 BiZact Open Sealer/Divider COVIDIEN
K130608 03/07/2013 QUADCUT MEDTRONIC NAVIGATION, INC.
K110751 03/18/2011 CODMAN BACTISEAL ENDOSCOPIC VENTICULAR CATHETER Codman & Shurtleff, Inc.
K171066 04/10/2017 BiZact Tonsillectomy Device Advanced Bipolar Tissue Sealer/Divider Covidien, llc
K211269 04/27/2021 Visualase MRI-Guided Laser Ablation System (SW 3.4) Medtronic Navigation, Inc.
K091346 05/07/2009 CODMAN HAKIM MICRO II VALVE Codman & Shurtleff, Inc.
K041421 05/28/2004 NAME BONE VOID FILLER STRYKER BIOTECH
K151649 06/18/2015 Valleylab FT10 Electrosurgical Platform COVIDIEN
K102589 09/09/2010 CODMAN BACTISEAL CATHETERS, CODMAN BACTISEAL EVD CATHETER Codman & Shurtleff, Inc.
K172757 09/13/2017 Valleylab FX8 Electrosurgical Platform Covidien llc
K143161 11/03/2014 Force FX-8(S), Force FX-8C(S), Force FX-8CA(S) COVIDIEN


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