EQUINOXE REVERSE SHOULDER SYSTEM FRACTURE HUMERAL ADAPTER TRAY AND LOCKING SCREW— 510(k) K073688

Substantially Equivalent

Exactech, Inc.

FDA 510(k) clearance K073688 for EQUINOXE REVERSE SHOULDER SYSTEM FRACTURE HUMERAL ADAPTER TRAY AND LOCKING SCREW, Substantially Equivalent on 2008-02-29. Applicant: Exactech, Inc..

Clearance details

Applicant: Exactech, Inc.
Product code: Code PHX
Advisory panel: Orthopedic
Date received: 2007-12-28
Decision date: 2008-02-29
Decision: Substantially Equivalent
Clearance type: Special
Location: Gainesville, FL, 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.