ACROMED/KANEDA ANTERIOR SPINAL INSTRUMENTATION— 510(k) K873826

Substantially Equivalent

Acromed Corp.

FDA 510(k) clearance K873826 for ACROMED/KANEDA ANTERIOR SPINAL INSTRUMENTATION, Substantially Equivalent on 1988-11-30. Applicant: Acromed Corp..

Clearance details

Applicant: Acromed Corp.
Product code: Code KWQ
Advisory panel: Orthopedic
Date received: 1987-09-23
Decision date: 1988-11-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Martinez, CA, 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.