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 |