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PIONEER ANTERIOR CERVICAL PLATE MODEL 24-SERIES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100708
510(k) Type
Traditional
Applicant
Pioneer Surgical Technology
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/2010
Days to Decision
84 days
Submission Type
Summary

PIONEER ANTERIOR CERVICAL PLATE MODEL 24-SERIES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100708
510(k) Type
Traditional
Applicant
Pioneer Surgical Technology
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/2010
Days to Decision
84 days
Submission Type
Summary