SMOOTH STAPLE IMPLANT— 510(k) K900433
UnknownInterphase Implants, Inc.
FDA 510(k) clearance K900433 for SMOOTH STAPLE IMPLANT, Unknown on 1990-11-16. Applicant: Interphase Implants, Inc.. Device class: 2.
Clearance details
- Applicant
- Interphase Implants, Inc.
- Product code
- Code MDL
- Device class
- Class 2
- Regulation
- 21 CFR 872.4760
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Livonia, MI, US
Recent devices under product code MDL
view allData sourced from openFDA. This site is unofficial and independent of the FDA.