Advanced Intramedullary Nail System— 510(k) K221221

Substantially Equivalent

Double Medical Technology, Inc.

FDA 510(k) clearance K221221 for Advanced Intramedullary Nail System, Substantially Equivalent on 2022-12-21. Applicant: Double Medical Technology, Inc..

Clearance details

Applicant
Double Medical Technology, Inc.
Product code
Code HSB
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Xiamen, CN
Download summary PDFView on FDA.gov ↗

Adverse events under product code HSB

product code HSB
Death
49
Injury
12,083
Malfunction
6,561
Other
1
Total
18,694

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.