Cook Biotech Incorporated - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
FDA 510(k) cleared devices by Cook Biotech Incorporated General & Plastic Surgery ✕
10 devices
Cleared
Jul 13, 2020
Biodesign Staple Line Reinforcement
General & Plastic Surgery
88d
Cleared
Dec 27, 2019
Biodesign Anal Fistula Plug, Biodesign Fistula Plug, Biodesign Plastic...
General & Plastic Surgery
185d
Cleared
Mar 13, 2018
Biodesign Diaphragmatic Hernia Graft
General & Plastic Surgery
267d
Cleared
Jul 10, 2017
Biodesign Parastomal Hernia Repair Graft
General & Plastic Surgery
263d
Cleared
Jun 21, 2017
Biodesign Fistula Plug
General & Plastic Surgery
169d
Cleared
Apr 28, 2017
Biodesign Staple Line Reinforcement
General & Plastic Surgery
29d
Cleared
Sep 28, 2016
Flowable Wound Matrix
General & Plastic Surgery
252d
Cleared
May 26, 2016
Biodesign Sling, Biodesign Plastic Surgery Matrix, Biodesign Anal Fistula Plug
General & Plastic Surgery
27d
Cleared
Apr 29, 2016
Biodesign Tissue Graft, Biodesign Dural Graft, Biodesign Peyronie's Repair...
General & Plastic Surgery
30d
Cleared
Aug 19, 2015
Cook ECM Powder
General & Plastic Surgery
28d