DEPUY CTA REVERSE SHOULDER SYSTEM— 510(k) K122442

Substantially Equivalent

Depuy France

FDA 510(k) clearance K122442 for DEPUY CTA REVERSE SHOULDER SYSTEM, Substantially Equivalent on 2012-09-06. Applicant: Depuy France.

Clearance details

Applicant: Depuy France
Product code: Code PHX
Advisory panel: Orthopedic
Date received: 2012-08-10
Decision date: 2012-09-06
Decision: Substantially Equivalent
Clearance type: Special
Location: Warsaw, IN, US

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Adverse events under product code PHX

product code PHX

Death: 10
Injury: 9,705
Malfunction: 1,252
Total: 10,967

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.