K063158

Substantially Equivalent

SYNTHES ANTEGRA SYSTEM

Applicant: Synthes Spine Co.Lp
Product code: KWQ
Advisory panel: Orthopedic
Date received: 2006-10-17
Decision date: 2006-11-14
Decision: Substantially Equivalent
Clearance type: Special
Location: West Chester, PA, US

Adverse events under product code KWQ

product code KWQ

Death: 8
Injury: 1,212
Malfunction: 1,233
Total: 2,453

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.