GEMINUS FOSSA SPECIFIC PLATE SYSTEM— 510(k) K122737

Substantially Equivalent

Skeletal Dynamics, LLC

FDA 510(k) clearance K122737 for GEMINUS FOSSA SPECIFIC PLATE SYSTEM, Substantially Equivalent on 2012-10-03. Applicant: Skeletal Dynamics, LLC.

Clearance details

Applicant: Skeletal Dynamics, LLC
Product code: Code HRS
Advisory panel: Orthopedic
Date received: 2012-09-06
Decision date: 2012-10-03
Decision: Substantially Equivalent
Clearance type: Special
Location: Miami, FL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code HRS

product code HRS

Death: 27
Injury: 10,340
Malfunction: 3,328
Total: 13,695

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.