K200073 is an FDA 510(k) clearance for the AugMENTA Penile Implant. This device is classified as a Elastomer, Silicone Block (Class II - Special Controls, product code MIB).
Submitted by Augmenta, LLC (Houston, US). The FDA issued a Cleared decision on September 30, 2022, 990 days after receiving the submission on January 14, 2020.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 874.3620.
| 510(k) Number | K200073 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 14, 2020 |
| Decision Date | September 30, 2022 |
| Days to Decision | 990 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | MIB - Elastomer, Silicone Block |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 874.3620 |