FDA 510(k), K072076, CYTOPLAST PTFE SUTURE

FDA 510(k), K072076, CYTOPLAST PTFE SUTURE

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510(K) Number: K072076
Device Name: CYTOPLAST PTFE SUTURE
Manufacturer: OSTEOGENICS BIOMEDICAL, INC.
Device Classification Name: suture, surgical, nonabsorbable, expanded, polytetraflouroethylene
Regulation Number: 878.5035
Classification Product Code: NBY
Date Received: 07/30/2007
Decision Date: 10/31/2007
Regulation Medical Specialty: General & Plastic Surgery
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