BIOPRO K-WIRE, MODELS 16863, 17231, 17232, 18577, 18682-18685— 510(k) K083490

Name: FDA 510(k) clearance K083490
Creator: U.S. Food and Drug Administration
Published: 2009-03-18

Substantially Equivalent

Biopro, Inc.

FDA 510(k) clearance K083490 for BIOPRO K-WIRE, MODELS 16863, 17231, 17232, 18577, 18682-18685, Substantially Equivalent on 2009-03-18. Applicant: Biopro, Inc.. Device class: 2.

Clearance details

Applicant: Biopro, Inc.
Product code: Code HTY
Device class: Class 2
Regulation: 21 CFR 888.3040
Advisory panel: Orthopedic
Date received: 2008-11-25
Decision date: 2009-03-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Port Huron, MI, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code HTY

product code HTY

Injury: 544
Total: 544

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.