Progressive Orthopaedic Total Knee System— 510(k) K150783

Substantially Equivalent

The Progressive Orthopaedic Company, LLC

FDA 510(k) clearance K150783 for Progressive Orthopaedic Total Knee System, Substantially Equivalent on 2015-06-23. Applicant: The Progressive Orthopaedic Company, LLC.

Clearance details

Applicant
The Progressive Orthopaedic Company, LLC
Product code
Code JWH
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
North Palm Beach, FL, US
Download summary PDFView on FDA.gov ↗

Adverse events under product code JWH

product code JWH
Death
26
Injury
51,564
Malfunction
9,725
Other
9
Total
61,324

Source: openFDA MAUDE database, through . 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.