ENDOBUTTON DIRECT— 510(k) K070167

Substantially Equivalent

Smith & Nephew Inc., Endoscopy Division

FDA 510(k) clearance K070167 for ENDOBUTTON DIRECT, Substantially Equivalent on 2007-04-12. Applicant: Smith & Nephew Inc., Endoscopy Division.

Clearance details

Applicant: Smith & Nephew Inc., Endoscopy Division
Product code: Code MBI
Advisory panel: Orthopedic
Date received: 2007-01-18
Decision date: 2007-04-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Andover, MA, 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.