Hominis Surgical System— 510(k) DEN190022
UnknownMomentis Surgical , Ltd.
FDA 510(k) clearance DEN190022 for Hominis Surgical System, Unknown on 2021-02-26. Applicant: Momentis Surgical , Ltd.. Device class: 2.
Clearance details
- Applicant
- Momentis Surgical , Ltd.
- Product code
- Code QNM
- Device class
- Class 2
- Regulation
- 21 CFR 878.4961
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Or Yehuda, IL
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