DR. HERZBERG DISPOSABLE EXTERNAL FIXATOR— 510(k) K890989

Name: FDA 510(k) clearance K890989
Creator: U.S. Food and Drug Administration
Published: 1990-04-05

Substantially Equivalent for Some Indications

Origin Medsystems, Inc.

FDA 510(k) clearance K890989 for DR. HERZBERG DISPOSABLE EXTERNAL FIXATOR, Substantially Equivalent for Some Indications on 1990-04-05. Applicant: Origin Medsystems, Inc.. Device class: 2.

Clearance details

Applicant: Origin Medsystems, Inc.
Product code: Code KTT
Device class: Class 2
Regulation: 21 CFR 888.3030
Advisory panel: Orthopedic
Date received: 1989-02-28
Decision date: 1990-04-05
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: San Mateo, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code KTT

product code KTT

Death: 11
Injury: 3,097
Malfunction: 1,261
Total: 4,369

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.