Percusys® Plus Pedicle Screw System— 510(k) K192680

Substantially Equivalent

Joimax GmbH

FDA 510(k) clearance K192680 for Percusys® Plus Pedicle Screw System, Substantially Equivalent on 2019-12-18. Applicant: Joimax GmbH.

Clearance details

Applicant: Joimax GmbH
Product code: Code NKB
Advisory panel: Orthopedic
Date received: 2019-09-26
Decision date: 2019-12-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Karlsruhe, DE

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.