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Healix™ Compression Screw System

Page Type
Cleared 510(K)
510(k) Number
K182949
510(k) Type
Traditional
Applicant
Nvision Biomedical Technologies, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/2018
Days to Decision
42 days
Submission Type
Summary

Healix™ Compression Screw System

Page Type
Cleared 510(K)
510(k) Number
K182949
510(k) Type
Traditional
Applicant
Nvision Biomedical Technologies, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/2018
Days to Decision
42 days
Submission Type
Summary