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PIONEER POSTERIOR OCCIPITO-CERVICO-THORACIC (OCT) SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121725
510(k) Type
Traditional
Applicant
Pioneer Surgical Technology, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/2012
Days to Decision
148 days
Submission Type
Summary

PIONEER POSTERIOR OCCIPITO-CERVICO-THORACIC (OCT) SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121725
510(k) Type
Traditional
Applicant
Pioneer Surgical Technology, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/2012
Days to Decision
148 days
Submission Type
Summary