CARDO MEDICAL FEMORAL CEMENT RESTRICTOR, MODEL 503-MCRX— 510(k) K101032

Substantially Equivalent

Cardo Medical, Inc.

FDA 510(k) clearance K101032 for CARDO MEDICAL FEMORAL CEMENT RESTRICTOR, MODEL 503-MCRX, Substantially Equivalent on 2010-07-08. Applicant: Cardo Medical, Inc..

Clearance details

Applicant: Cardo Medical, Inc.
Product code: Code JWH
Advisory panel: Orthopedic
Date received: 2010-04-14
Decision date: 2010-07-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clifton, NJ, US

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Adverse events under product code JWH

product code JWH

Death: 26
Injury: 51,564
Malfunction: 9,725
Other: 9
Total: 61,324

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.