SANTIS PEDICLE SCREW SYSTEM— 510(k) K133063

Substantially Equivalent

Lanterna Medical Technologies

FDA 510(k) clearance K133063 for SANTIS PEDICLE SCREW SYSTEM, Substantially Equivalent on 2014-01-13. Applicant: Lanterna Medical Technologies.

Clearance details

Applicant: Lanterna Medical Technologies
Product code: Code NKB
Advisory panel: Orthopedic
Date received: 2013-09-27
Decision date: 2014-01-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Apple Valley, MN, US

Download summary PDF View 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, 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.