HemiCAP Humeral Head XL (HHXL) Articular Resurfacing System— 510(k) K142942

Substantially Equivalent

Arthrosurface, Inc.

FDA 510(k) clearance K142942 for HemiCAP Humeral Head XL (HHXL) Articular Resurfacing System, Substantially Equivalent on 2014-12-19. Applicant: Arthrosurface, Inc..

Clearance details

Applicant: Arthrosurface, Inc.
Product code: Code HSD
Advisory panel: Orthopedic
Date received: 2014-10-14
Decision date: 2014-12-19
Decision: Substantially Equivalent
Clearance type: Special
Location: Franklin, MA, US

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Adverse events under product code HSD

product code HSD

Injury: 3,425
Malfunction: 531
Total: 3,956

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.