MOTOR DRIVEN EXTIRPATION INSTRUMENTS— 510(k) K904859

Name: FDA 510(k) clearance K904859
Creator: U.S. Food and Drug Administration
Published: 1991-03-15

Substantially Equivalent

Aesculap, Inc.

FDA 510(k) clearance K904859 for MOTOR DRIVEN EXTIRPATION INSTRUMENTS, Substantially Equivalent on 1991-03-15. Applicant: Aesculap, Inc.. Device class: 2.

Clearance details

Applicant: Aesculap, Inc.
Product code: Code HRX
Device class: Class 2
Regulation: 21 CFR 888.1100
Advisory panel: Orthopedic
Date received: 1990-10-29
Decision date: 1991-03-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Burlingame, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code HRX

product code HRX

Injury: 623
Malfunction: 11,257
Total: 11,880

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.