LDR SPINE USA C-PLATE, TL ANTERIOR CERVICAL PLATE SYSTEM— 510(k) K102265

Substantially Equivalent

Ldr Spine USA

FDA 510(k) clearance K102265 for LDR SPINE USA C-PLATE, TL ANTERIOR CERVICAL PLATE SYSTEM, Substantially Equivalent on 2010-09-29. Applicant: Ldr Spine USA.

Clearance details

Applicant: Ldr Spine USA
Product code: Code KWQ
Advisory panel: Orthopedic
Date received: 2010-08-10
Decision date: 2010-09-29
Decision: Substantially Equivalent
Clearance type: Special
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.