INTEGRA EXPANDABLE INTERVEREBRAL BODY FUSION DEVICE (IBD) SYSTEM— 510(k) K133418

Substantially Equivalent

Seaspine, Inc.

FDA 510(k) clearance K133418 for INTEGRA EXPANDABLE INTERVEREBRAL BODY FUSION DEVICE (IBD) SYSTEM, Substantially Equivalent on 2014-05-01. Applicant: Seaspine, Inc..

Clearance details

Applicant: Seaspine, Inc.
Product code: Code MAX
Advisory panel: Orthopedic
Date received: 2013-11-07
Decision date: 2014-05-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Vista, CA, US

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Adverse events under product code MAX

product code MAX

Death: 13
Injury: 1,305
Malfunction: 2,885
Total: 4,203

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.