VERTETRAC— 510(k) K771988

Substantially Equivalent

Ballert Orthopedic Corp.

FDA 510(k) clearance K771988 for VERTETRAC, Substantially Equivalent on 1979-02-01. Applicant: Ballert Orthopedic Corp..

Clearance details

Applicant: Ballert Orthopedic Corp.
Product code: Code HST
Advisory panel: Orthopedic
Date received: 1977-10-19
Decision date: 1979-02-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code HST

product code HST

Other: 1
Total: 1

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.