CrossFT Knotless Deep Thread Suture Anchor with Disposable Driver— 510(k) K182621

Substantially Equivalent

Conmed Corporation

FDA 510(k) clearance K182621 for CrossFT Knotless Deep Thread Suture Anchor with Disposable Driver, Substantially Equivalent on 2019-01-04. Applicant: Conmed Corporation.

Clearance details

Applicant: Conmed Corporation
Product code: Code MBI
Advisory panel: Orthopedic
Date received: 2018-09-24
Decision date: 2019-01-04
Decision: Substantially Equivalent
Clearance type: Special
Location: Utica, NY, 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.