CONMED LINVATEC XO BUTTON— 510(k) K070780

Substantially Equivalent

Conmed Linvatec

FDA 510(k) clearance K070780 for CONMED LINVATEC XO BUTTON, Substantially Equivalent on 2007-08-21. Applicant: Conmed Linvatec.

Clearance details

Applicant: Conmed Linvatec
Product code: Code MBI
Advisory panel: Orthopedic
Date received: 2007-03-21
Decision date: 2007-08-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Largo, FL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code MBI

product code MBI

Injury: 3,163
Malfunction: 13,006
Other: 2
Total: 16,171

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.