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Healix Compression Screw System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K200914
510(k) Type
Special
Applicant
Nvision Biomedical Technologies, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/2020
Days to Decision
29 days
Submission Type
Summary

Healix Compression Screw System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K200914
510(k) Type
Special
Applicant
Nvision Biomedical Technologies, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/2020
Days to Decision
29 days
Submission Type
Summary