The following data is part of a premarket notification filed by American Medical Systems, Inc. with the FDA for Ams Ambicor Penile Prosthesis.
| Device ID | K963328 |
| 510k Number | K963328 |
| Device Name: | AMS AMBICOR PENILE PROSTHESIS |
| Classification | Prosthesis, Penile |
| Applicant | AMERICAN MEDICAL SYSTEMS, INC. 10700 BREN RD., WEST Minnetonka, MN 55343 |
| Contact | Kris Teich |
| Correspondent | Kris Teich AMERICAN MEDICAL SYSTEMS, INC. 10700 BREN RD., WEST Minnetonka, MN 55343 |
| Product Code | FAE |
| CFR Regulation Number | 876.3630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-08-23 |
| Decision Date | 1996-12-04 |
| Summary: | summary |