SOFT TISSUE AUGMENTATION TUBE


Device Classification Name

mesh, surgical, polymeric

510(k) Number K960481
Device Name SOFT TISSUE AUGMENTATION TUBE
Applicant
TISSUE TECHNOLOGIES, INC.
1370 green st.
san franciso, 
CA 
94109

Applicant Contact jesse kramer
Correspondent
TISSUE TECHNOLOGIES, INC.
1370 green st.
san franciso, 
CA 
94109

Correspodent Contact jesse kramer
Regulation Number 878.3300
Classification Product Code
FTL  
Date Received 02/02/1996
Decision Date 04/01/1996
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General & Plastic Surgery

510k Review Panel

General & Plastic Surgery

Type Traditional
Reviewed by Third Party No

Combination Product

No

Category: Uncategorized