The following data is part of a premarket notification filed by Sientra, Inc with the FDA for Sientra Opus Silicone Gel Breast Implant Sizer.
| Device ID | K200706 |
| 510k Number | K200706 |
| Device Name: | Sientra OPUS Silicone Gel Breast Implant Sizer |
| Classification | Sizer, Mammary, Breast Implant Volume |
| Applicant | Sientra, Inc 420 South Fairview Avenue, Suite 200 Santa Barbara, CA 93117 |
| Contact | Joann Kuhne |
| Correspondent | Joann Kuhne Sientra, Inc 420 South Fairview Avenue, Suite 200 Santa Barbara, CA 93117 |
| Product Code | MRD |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2020-03-18 |
| Decision Date | 2020-11-16 |
| Summary: | summary |