CrossFT Knotless Biocomposite Suture Anchor with Disposable Driver— 510(k) K170501

Substantially Equivalent

Conmed Corporation

FDA 510(k) clearance K170501 for CrossFT Knotless Biocomposite Suture Anchor with Disposable Driver, Substantially Equivalent on 2017-03-17. Applicant: Conmed Corporation.

Clearance details

Applicant: Conmed Corporation
Product code: Code MAI
Advisory panel: Orthopedic
Date received: 2017-02-21
Decision date: 2017-03-17
Decision: Substantially Equivalent
Clearance type: Special
Location: Utica, NY, US

Download summary PDF View on FDA.gov ↗

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.