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MAXIMA ANTERIOR CERVICAL PLATE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061002
510(k) Type
Traditional
Applicant
U&I CORP.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
11/15/2006
Days to Decision
218 days
Submission Type
Summary

MAXIMA ANTERIOR CERVICAL PLATE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061002
510(k) Type
Traditional
Applicant
U&I CORP.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
11/15/2006
Days to Decision
218 days
Submission Type
Summary