INDUS ANTERIOR CERVICAL PLATE SYSTEM, MODEL IM3XXX— 510(k) K073232

Substantially Equivalent

Spinefrontier, Inc.

FDA 510(k) clearance K073232 for INDUS ANTERIOR CERVICAL PLATE SYSTEM, MODEL IM3XXX, Substantially Equivalent on 2008-02-20. Applicant: Spinefrontier, Inc..

Clearance details

Applicant: Spinefrontier, Inc.
Product code: Code KWQ
Advisory panel: Orthopedic
Date received: 2007-11-15
Decision date: 2008-02-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Beverly, MA, US

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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.