FASTX STERNAL INTRAOSSEOUS DEVICE— 510(k) K100124

Substantially Equivalent

Pyng Medical Corp.

FDA 510(k) clearance K100124 for FASTX STERNAL INTRAOSSEOUS DEVICE, Substantially Equivalent on 2010-08-31. Applicant: Pyng Medical Corp..

Clearance details

Applicant: Pyng Medical Corp.
Product code: Code FMI
Advisory panel: General Hospital
Date received: 2010-01-19
Decision date: 2010-08-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Richmond, Bc, CA

Download summary PDF View on FDA.gov ↗

Adverse events under product code FMI

product code FMI

Death: 28
Injury: 1,517
Malfunction: 23,981
Other: 18
Total: 25,544

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.