510(k) K896941

AMS DYNAFLEX SELF CONTAINED PENILE PROSTHESIS by American Medical Systems, Inc. — Product Code FAE

K896941 is an FDA 510(k) premarket notification submitted by American Medical Systems, Inc. for the device "AMS DYNAFLEX SELF CONTAINED PENILE PROSTHESIS". The FDA issued a decision of Substantially Equivalent on March 6, 1990. The device falls under product code FAE (Prosthesis, Penile), a Class II device regulated under 21 CFR 876.3630. American Medical Systems, Inc. has at least 10 other 510(k) clearances on record.