CD Horizon™ Spinal System— 510(k) K210637

Substantially Equivalent

Medtronic

FDA 510(k) clearance K210637 for CD Horizon™ Spinal System, Substantially Equivalent on 2021-04-30. Applicant: Medtronic.

Clearance details

Applicant
Medtronic
Product code
Code NKB
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Memphis, TN, US
Download summary PDFView on FDA.gov ↗

Adverse events under product code NKB

product code NKB
Death
27
Injury
5,033
Malfunction
4,140
Total
9,200

Source: openFDA MAUDE database, through . 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.