BARD ENDO LINK INTRACONDYLAR ROTATING— 510(k) K821476

Substantially Equivalent

C.R. Bard, Inc.

FDA 510(k) clearance K821476 for BARD ENDO LINK INTRACONDYLAR ROTATING, Substantially Equivalent on 1982-06-23. Applicant: C.R. Bard, Inc..

Clearance details

Applicant: C.R. Bard, Inc.
Product code: Code KRO
Advisory panel: Orthopedic
Date received: 1982-05-18
Decision date: 1982-06-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code KRO

product code KRO

Death: 19
Injury: 4,841
Total: 4,860

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.