Customized Contour Implant— 510(k) K191130
Substantially EquivalentImplantech Associates, Inc.
FDA 510(k) clearance K191130 for Customized Contour Implant, Substantially Equivalent on 2019-08-23. Applicant: Implantech Associates, Inc.. Device class: 2.
Clearance details
- Applicant
- Implantech Associates, Inc.
- Product code
- Code FWP
- Device class
- Class 2
- Regulation
- 21 CFR 878.3550
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Ventura, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.