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PIONEER VERTEBRAL SPACER (VERTEBRAL SPACER)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061151
510(k) Type
Traditional
Applicant
Pioneer Surgical Technology
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/2006
Days to Decision
90 days
Submission Type
Summary

PIONEER VERTEBRAL SPACER (VERTEBRAL SPACER)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061151
510(k) Type
Traditional
Applicant
Pioneer Surgical Technology
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/2006
Days to Decision
90 days
Submission Type
Summary