K171592

Substantially Equivalent

CrossFT Knotless Biocomposite Suture Anchor with Disposable Driver

Applicant: Conmed Corporation
Product code: MAI
Advisory panel: Orthopedic
Date received: 2017-05-31
Decision date: 2017-08-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Utica, NY, US

Adverse events under product code MAI

product code MAI

Injury: 1,948
Malfunction: 8,580
Total: 10,528

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.