Trinity PLUS Acetabular Shell— 510(k) K172551
Substantially EquivalentCorin U.S.A. Limited
FDA 510(k) clearance K172551 for Trinity PLUS Acetabular Shell, Substantially Equivalent on 2018-06-15. Applicant: Corin U.S.A. Limited.
Clearance details
- Applicant
- Corin U.S.A. Limited
- Product code
- Code LPH
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tampa, FL, US
Adverse events under product code LPH
product code LPH- Death
- 73
- Injury
- 31,640
- Malfunction
- 3,358
- Other
- 2
- Total
- 35,073
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.