Cook Biotech Incorporated
Cook Biotech Incorporated holds FDA 510(k) medical device clearances, first cleared 2013, most recent 2024.
Top product codes for Cook Biotech Incorporated
Recent clearances by Cook Biotech Incorporated
- K232646 — Biodesign Otologic Butterfly Graft (ENT-OTO-BFLY-0.4-0.6); Biodesign Otologic Butterfly Graft (ENT-OTO-BFLY-0.6-0.9)
- K201000 — Biodesign Staple Line Reinforcement
- K191696 — Biodesign Anal Fistula Plug, Biodesign Fistula Plug, Biodesign Plastic Surgery Matrix, Biodesign Tissue Graft
- K171817 — Biodesign Diaphragmatic Hernia Graft
- K162934 — Biodesign Parastomal Hernia Repair Graft
- K170016 — Biodesign Fistula Plug
- K170945 — Biodesign Staple Line Reinforcement
- K161762 — DynaMatrix/Dynamatrix Plus
- K162741 — AxoGuard Nerve Connector
- K160136 — Flowable Wound Matrix
- K161221 — Biodesign Sling, Biodesign Plastic Surgery Matrix, Biodesign Anal Fistula Plug
- K161000 — Biodesign Otologic Repair Graft
- K160869 — Biodesign Tissue Graft, Biodesign Dural Graft, Biodesign Peyronie's Repair Graft
- K152033 — Cook ECM Powder
- K132660 — NERVE CUFF
- K130006 — BIODESIGN SURGISIS ANTERIOR POSTERIOR PELVIC FLOOR GRAFTS
Data sourced from openFDA. This site is unofficial and independent of the FDA.