SpeedLock Knotless Fixation System— 510(k) K153313

Substantially Equivalent

ArthroCare Corporation

FDA 510(k) clearance K153313 for SpeedLock Knotless Fixation System, Substantially Equivalent on 2015-12-11. Applicant: ArthroCare Corporation.

Clearance details

Applicant: ArthroCare Corporation
Product code: Code MBI
Advisory panel: Orthopedic
Date received: 2015-11-17
Decision date: 2015-12-11
Decision: Substantially Equivalent
Clearance type: Special
Location: Irvine, CA, 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.