TRIPORE TDD (HA), TRIPORE TDD (BP90), TRIPORE TDD (BP15)— 510(k) K110787

Substantially Equivalent

Orthogem Limited

FDA 510(k) clearance K110787 for TRIPORE TDD (HA), TRIPORE TDD (BP90), TRIPORE TDD (BP15), Substantially Equivalent on 2011-04-21. Applicant: Orthogem Limited.

Clearance details

Applicant: Orthogem Limited
Product code: Code MQV
Advisory panel: Orthopedic
Date received: 2011-03-21
Decision date: 2011-04-21
Decision: Substantially Equivalent
Clearance type: Special
Location: Nottingham, GB

Download summary PDF View on FDA.gov ↗

Adverse events under product code MQV

product code MQV

Death: 6
Injury: 435
Total: 441

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. 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.