GENESYS SPINE ANTERIOR CERVICAL PLATE SYSTEM— 510(k) K111132

Substantially Equivalent

Genesys Spine

FDA 510(k) clearance K111132 for GENESYS SPINE ANTERIOR CERVICAL PLATE SYSTEM, Substantially Equivalent on 2011-12-09. Applicant: Genesys Spine.

Clearance details

Applicant: Genesys Spine
Product code: Code KWQ
Advisory panel: Orthopedic
Date received: 2011-04-22
Decision date: 2011-12-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Austin, TX, 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.