Clearance Summary
Dignitana AB DigniCap System received FDA 510(k) clearance under submission number DEN150010, sponsored by Dignitana AB. The device was reviewed via the Direct premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2015-12-08.
- Submission: DEN150010
- Applicant / Sponsor: Dignitana AB
- Clearance pathway: Direct
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4360
- Decision date: 2015-12-08
Classification & Regulation
This clearance is catalogued under FDA product code PMC and 21 CFR 878.4360, within the General, Plastic Surgery review panel as a Class II device.