K941605

Substantially Equivalent

STRYKER FEMORAL CANAL BRUSH, ACETABULAR BRUSH

Applicant: Stryker Corp.
Product code: LXH
Advisory panel: Orthopedic
Date received: 1994-04-01
Decision date: 1994-08-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kalamazoo, MI, US

Adverse events under product code LXH

product code LXH

Death: 11
Injury: 2,218
Malfunction: 31,318
Total: 33,547

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.