SYNTHES SPINE PEDIATRIC ROD SYSTEM— 510(k) K980761

Substantially Equivalent

Synthes Spine

FDA 510(k) clearance K980761 for SYNTHES SPINE PEDIATRIC ROD SYSTEM, Substantially Equivalent on 1998-08-04. Applicant: Synthes Spine.

Clearance details

Applicant: Synthes Spine
Product code: Code MNH
Advisory panel: Orthopedic
Date received: 1998-02-27
Decision date: 1998-08-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Paoli, PA, US

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Adverse events under product code MNH

product code MNH

Injury: 978
Malfunction: 793
Total: 1,771

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.