NEXLOCK FEMORAL STEM— 510(k) K955171

Substantially Equivalent

Nexmed, Inc.

FDA 510(k) clearance K955171 for NEXLOCK FEMORAL STEM, Substantially Equivalent on 1996-02-09. Applicant: Nexmed, Inc..

Clearance details

Applicant: Nexmed, Inc.
Product code: Code JDG
Advisory panel: Orthopedic
Date received: 1995-11-13
Decision date: 1996-02-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Palm Desert, CA, US

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Adverse events under product code JDG

product code JDG

Injury: 804
Malfunction: 3,242
Total: 4,046

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.