OmniPore DUROMAX Surgical Implants— 510(k) K180249
Substantially EquivalentMatrix Surgical Holdings, LLC/Matrix Surgical USA
FDA 510(k) clearance K180249 for OmniPore DUROMAX Surgical Implants, Substantially Equivalent on 2018-10-11. Applicant: Matrix Surgical Holdings, LLC/Matrix Surgical USA. Device class: 2.
Clearance details
- Applicant
- Matrix Surgical Holdings, LLC/Matrix Surgical USA
- Product code
- Code JEY
- Device class
- Class 2
- Regulation
- 21 CFR 872.4760
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Atlanta, GA, US
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More clearances from Matrix Surgical Holdings, LLC/Matrix Surgical USA
view allAdverse events under product code JEY
product code JEY- Injury
- 1,542
- Malfunction
- 2,292
- Total
- 3,834
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.