B-TWIN BONE EXPANDER SYSTEM (B-TWIN BE SYSTEM)— 510(k) K032358

Name: FDA 510(k) clearance K032358
Creator: U.S. Food and Drug Administration
Published: 2003-12-17

Substantially Equivalent

Disc-O-Tech Medical Technologies, Ltd.

FDA 510(k) clearance K032358 for B-TWIN BONE EXPANDER SYSTEM (B-TWIN BE SYSTEM), Substantially Equivalent on 2003-12-17. Applicant: Disc-O-Tech Medical Technologies, Ltd.. Device class: 2.

Clearance details

Applicant: Disc-O-Tech Medical Technologies, Ltd.
Product code: Code HRX
Device class: Class 2
Regulation: 21 CFR 888.1100
Advisory panel: Orthopedic
Date received: 2003-07-30
Decision date: 2003-12-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, 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.