BIOPRO KWICK-WIRE UNIVERSAL SCREW SYSTEM— 510(k) K130298

Substantially Equivalent

Biopro, Inc.

FDA 510(k) clearance K130298 for BIOPRO KWICK-WIRE UNIVERSAL SCREW SYSTEM, Substantially Equivalent on 2013-06-18. Applicant: Biopro, Inc..

Clearance details

Applicant: Biopro, Inc.
Product code: Code JDW
Advisory panel: Orthopedic
Date received: 2013-02-07
Decision date: 2013-06-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Prior Lake, MN, US

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Adverse events under product code JDW

product code JDW

Injury: 717
Total: 717

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.