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ONX Large External Fixation System

Page Type
Cleared 510(K)
510(k) Number
K213905
510(k) Type
Traditional
Applicant
OrthoNovis, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/2022
Days to Decision
254 days
Submission Type
Summary

ONX Large External Fixation System

Page Type
Cleared 510(K)
510(k) Number
K213905
510(k) Type
Traditional
Applicant
OrthoNovis, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/2022
Days to Decision
254 days
Submission Type
Summary