SYNTHES STERNAL FIXATION SYSTEM— 510(k) K093772

Substantially Equivalent

Synthes

FDA 510(k) clearance K093772 for SYNTHES STERNAL FIXATION SYSTEM, Substantially Equivalent on 2010-03-29. Applicant: Synthes.

Clearance details

Applicant: Synthes
Product code: Code HRS
Advisory panel: Orthopedic
Date received: 2009-12-08
Decision date: 2010-03-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Chester, PA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code HRS

product code HRS

Death: 27
Injury: 10,340
Malfunction: 3,328
Total: 13,695

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.