FDA 510(k), K100593, SUTURE PLACEMENT DEVICE AND ACCESSORIES, FLEXIBLE SUTURE PLACEMENT DEVICE AND ACCESSORIES, LSI R SERIES SUTURE PLACEME

FDA 510(k), K100593, SUTURE PLACEMENT DEVICE AND ACCESSORIES, FLEXIBLE SUTURE PLACEMENT DEVICE AND ACCESSORIES, LSI R SERIES SUTURE PLACEME

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510(K) Number: K100593
Device Name: SUTURE PLACEMENT DEVICE AND ACCESSORIES, FLEXIBLE SUTURE PLACEMENT DEVICE AND ACCESSORIES, LSI R SERIES SUTURE PLACEME
Manufacturer: LSI SOLUTIONS, INC.
Device Classification Name: suture, nonabsorbable, synthetic, polypropylene
Regulation Number: 878.5010
Classification Product Code: GAW
Date Received: 03/02/2010
Decision Date: 10/13/2010
Regulation Medical Specialty: General & Plastic Surgery

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