PIONEER ANTERIOR CERVICAL PLATE MODEL 24-SERIES— 510(k) K100708

Substantially Equivalent

Pioneer Surgical Technology

FDA 510(k) clearance K100708 for PIONEER ANTERIOR CERVICAL PLATE MODEL 24-SERIES, Substantially Equivalent on 2010-06-04. Applicant: Pioneer Surgical Technology.

Clearance details

Applicant: Pioneer Surgical Technology
Product code: Code KWQ
Advisory panel: Orthopedic
Date received: 2010-03-12
Decision date: 2010-06-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Marquette, MI, US

Download summary PDF View on FDA.gov ↗

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.