nvc— 510(k) K190380

Substantially Equivalent

Nvision Biomedical Technologies, Inc.

FDA 510(k) clearance K190380 for nvc, Substantially Equivalent on 2019-03-21. Applicant: Nvision Biomedical Technologies, Inc..

Clearance details

Applicant: Nvision Biomedical Technologies, Inc.
Product code: Code ODP
Advisory panel: Orthopedic
Date received: 2019-02-19
Decision date: 2019-03-21
Decision: Substantially Equivalent
Clearance type: Special
Location: San Antonio, TX, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code ODP

product code ODP

Injury: 310
Total: 310

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.