SYNTHES POSTERIOR UNIVERSAL SPINAL SYSTEM— 510(k) K982987

Substantially Equivalent

Synthes Spine

FDA 510(k) clearance K982987 for SYNTHES POSTERIOR UNIVERSAL SPINAL SYSTEM, Substantially Equivalent on 1998-10-21. Applicant: Synthes Spine.

Clearance details

Applicant: Synthes Spine
Product code: Code MNI
Advisory panel: Orthopedic
Date received: 1998-08-26
Decision date: 1998-10-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Paoli, PA, US

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Adverse events under product code MNI

product code MNI

Injury: 641
Total: 641

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.