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EARP Interbody System

Page Type
Cleared 510(K)
510(k) Number
K212477
510(k) Type
Traditional
Applicant
Nvision Biomedical Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/2022
Days to Decision
262 days
Submission Type
Summary

EARP Interbody System

Page Type
Cleared 510(K)
510(k) Number
K212477
510(k) Type
Traditional
Applicant
Nvision Biomedical Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/2022
Days to Decision
262 days
Submission Type
Summary