KAR— 510(k) K961732

Substantially Equivalent

Landos, Inc.

FDA 510(k) clearance K961732 for KAR, Substantially Equivalent on 1997-07-08. Applicant: Landos, Inc..

Clearance details

Applicant: Landos, Inc.
Product code: Code MEH
Advisory panel: Orthopedic
Date received: 1996-05-03
Decision date: 1997-07-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Potomac, MD, 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.