KARL STORZ MEGAFIX-T TITANIUM INTERFERENCE SCREW— 510(k) K030368

Substantially Equivalent

KARL STORZ Endoscopy-America, Inc.

FDA 510(k) clearance K030368 for KARL STORZ MEGAFIX-T TITANIUM INTERFERENCE SCREW, Substantially Equivalent on 2003-03-20. Applicant: KARL STORZ Endoscopy-America, Inc..

Clearance details

Applicant: KARL STORZ Endoscopy-America, Inc.
Product code: Code HWC
Advisory panel: Orthopedic
Date received: 2003-02-04
Decision date: 2003-03-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Culver City, CA, US

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.