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CANNULATED SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K003496
510(k) Type
Traditional
Applicant
PIONEER SURGICAL TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/2001
Days to Decision
87 days
Submission Type
Summary

CANNULATED SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K003496
510(k) Type
Traditional
Applicant
PIONEER SURGICAL TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/2001
Days to Decision
87 days
Submission Type
Summary