510(k) K955599— STRYKER FEMORAL CANAL SPONGE & ACETABULUM SPONGE

Substantially Equivalent

Stryker Corp.

Clearance details

Applicant: Stryker Corp.
Product code: Code GDY
Advisory panel: General, Plastic Surgery
Date received: 1995-12-08
Decision date: 1996-02-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kalamazoo, MI, US

Adverse events under product code GDY

product code GDY

Malfunction: 764
Total: 764

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.