Cook Biotech Incorporated
FDA 510(k) medical device clearances.
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.