STRYKER TITANIUM CROSS-SCREW SYSTEM, MODEL 234-500-1XX— 510(k) K011319

Substantially Equivalent

Stryker Endoscopy

FDA 510(k) clearance K011319 for STRYKER TITANIUM CROSS-SCREW SYSTEM, MODEL 234-500-1XX, Substantially Equivalent on 2001-07-20. Applicant: Stryker Endoscopy.

Clearance details

Applicant: Stryker Endoscopy
Product code: Code JDW
Advisory panel: Orthopedic
Date received: 2001-05-01
Decision date: 2001-07-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Clara, CA, US

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Adverse events under product code JDW

product code JDW

Injury: 717
Total: 717

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.