KANEDA ANTERIOR SPINAL MULTISEGMENTAL FIXATION DEV— 510(k) K923703

Substantially Equivalent for Some Indications

Acromed Corp.

FDA 510(k) clearance K923703 for KANEDA ANTERIOR SPINAL MULTISEGMENTAL FIXATION DEV, Substantially Equivalent for Some Indications on 1993-05-20. Applicant: Acromed Corp..

Clearance details

Applicant: Acromed Corp.
Product code: Code KWQ
Advisory panel: Orthopedic
Date received: 1992-07-24
Decision date: 1993-05-20
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Cleveland, OH, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code KWQ

product code KWQ

Death: 8
Injury: 1,212
Malfunction: 1,233
Total: 2,453

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.