STRYKER STAPLER SYSTEM— 510(k) K931103

Substantially Equivalent

Stryker Endoscopy

FDA 510(k) clearance K931103 for STRYKER STAPLER SYSTEM, Substantially Equivalent on 1993-10-12. Applicant: Stryker Endoscopy.

Clearance details

Applicant: Stryker Endoscopy
Product code: Code GDW
Advisory panel: General, Plastic Surgery
Date received: 1993-03-03
Decision date: 1993-10-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Jose, CA, US

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Adverse events under product code GDW

product code GDW

Death: 450
Injury: 12,684
Malfunction: 68,730
Other: 6
Total: 81,870

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.