OLECRA INTRAMEDULLARY FIXATION SYSTEM— 510(k) K110322

Substantially Equivalent

Mylad Orthopedic Solutions

FDA 510(k) clearance K110322 for OLECRA INTRAMEDULLARY FIXATION SYSTEM, Substantially Equivalent on 2011-03-04. Applicant: Mylad Orthopedic Solutions.

Clearance details

Applicant: Mylad Orthopedic Solutions
Product code: Code HSB
Advisory panel: Orthopedic
Date received: 2011-02-03
Decision date: 2011-03-04
Decision: Substantially Equivalent
Clearance type: Special
Location: Mclean, VA, US

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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, 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.