PERMA FACIAL IMPLANTS— 510(k) K071823
Substantially EquivalentSurgisil
FDA 510(k) clearance K071823 for PERMA FACIAL IMPLANTS, Substantially Equivalent on 2007-09-19. Applicant: Surgisil. Device class: 2.
Clearance details
- Applicant
- Surgisil
- Product code
- Code ODU
- Device class
- Class 2
- Regulation
- 21 CFR 878.3500
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- North Attleboro, MA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.