ACROSSPINE PEDICLE SCREW SYSTEM— 510(k) K141695

Substantially Equivalent

Arthro-Dif

FDA 510(k) clearance K141695 for ACROSSPINE PEDICLE SCREW SYSTEM, Substantially Equivalent on 2014-12-30. Applicant: Arthro-Dif.

Clearance details

Applicant: Arthro-Dif
Product code: Code NKB
Advisory panel: Orthopedic
Date received: 2014-06-24
Decision date: 2014-12-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fr. Myers, FL, 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.