HA TI-FIT ACETABULAR AND FEMORAL COMPONENT— 510(k) K922621

Substantially Equivalent for Some Indications

Smith & Nephew Richards, Inc.

FDA 510(k) clearance K922621 for HA TI-FIT ACETABULAR AND FEMORAL COMPONENT, Substantially Equivalent for Some Indications on 1994-03-17. Applicant: Smith & Nephew Richards, Inc..

Clearance details

Applicant: Smith & Nephew Richards, Inc.
Product code: Code MEH
Advisory panel: Orthopedic
Date received: 1992-06-03
Decision date: 1994-03-17
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Memphis, TN, US

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Adverse events under product code MEH

product code MEH

Injury: 2,021
Total: 2,021

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.