AAP CANNULATED SCREW AND DARCO HEADED SCREW— 510(k) K080101

Substantially Equivalent

Aap Implantate AG

FDA 510(k) clearance K080101 for AAP CANNULATED SCREW AND DARCO HEADED SCREW, Substantially Equivalent on 2008-03-25. Applicant: Aap Implantate AG.

Clearance details

Applicant: Aap Implantate AG
Product code: Code HWC
Advisory panel: Orthopedic
Date received: 2008-01-14
Decision date: 2008-03-25
Decision: Substantially Equivalent
Clearance type: Special
Location: Berlin, DE

Download summary PDF View on FDA.gov ↗

Adverse events under product code HWC

product code HWC

Death: 20
Injury: 15,910
Malfunction: 8,192
Other: 1
Total: 24,123

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.