AESCULAP IMPLANT SYSTEMS S4 SPINAL SYSTEM— 510(k) K100623

Substantially Equivalent

Aesculap Implant Systems

FDA 510(k) clearance K100623 for AESCULAP IMPLANT SYSTEMS S4 SPINAL SYSTEM, Substantially Equivalent on 2010-06-09. Applicant: Aesculap Implant Systems.

Clearance details

Applicant: Aesculap Implant Systems
Product code: Code NKB
Advisory panel: Orthopedic
Date received: 2010-03-04
Decision date: 2010-06-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Center Valley, PA, 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.