K070908

Substantially Equivalent

SMITH & NEPHEW KINSA RC SUTURE ANCHOR

Applicant: Smith & Nephew Inc., Endoscopy Division
Product code: MBI
Advisory panel: Orthopedic
Date received: 2007-04-02
Decision date: 2007-05-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Andover, MA, US

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.