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FDA 510(k) K050516, T-SLING, by Herniamesh S.R.L.

FDA 510(k) K050516, T-SLING, by Herniamesh S.R.L.

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510(K) Number: K050516
Device Name: T-SLING
Manufacturer: Herniamesh S.R.L.
Device Classification Name: mesh, surgical, synthetic, urogynecologic, for stress urinary incontinence, retropubic or transobturator
Regulation Number: 878.3300
Classification Product Code: OTN
Date Received: 03/01/2005
Decision Date: 02/03/2006
Regulation Medical Specialty: General & Plastic Surgery
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