H-220 PRESS-FIT ACETABULAR CUP SYSTEM— 510(k) K926134

Substantially Equivalent

Implex Corp.

FDA 510(k) clearance K926134 for H-220 PRESS-FIT ACETABULAR CUP SYSTEM, Substantially Equivalent on 1993-10-15. Applicant: Implex Corp..

Clearance details

Applicant: Implex Corp.
Product code: Code MEH
Advisory panel: Orthopedic
Date received: 1992-12-07
Decision date: 1993-10-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Allendale, NJ, 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.