Tyber Medical Staple Fixation System (various)— 510(k) K221947
Substantially EquivalentTyber Medical, LLC
FDA 510(k) clearance K221947 for Tyber Medical Staple Fixation System (various), Substantially Equivalent on 2022-10-20. Applicant: Tyber Medical, LLC.
Clearance details
- Applicant
- Tyber Medical, LLC
- Product code
- Code JDR
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bethlehem, PA, US
Adverse events under product code JDR
product code JDR- Injury
- 726
- Malfunction
- 663
- Other
- 1
- Total
- 1,390
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.