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ANAX™ OCT Spinal System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183383
510(k) Type
Special
Applicant
U & I Corporation
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
12/12/2018
Days to Decision
6 days
Submission Type
Summary

ANAX™ OCT Spinal System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183383
510(k) Type
Special
Applicant
U & I Corporation
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
12/12/2018
Days to Decision
6 days
Submission Type
Summary