Last synced on 14 November 2025 at 11:06 pm

PIONEER CANNULATED SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K102903
510(k) Type
Special
Applicant
PIONEER SURGICAL TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/2010
Days to Decision
20 days
Submission Type
Summary

PIONEER CANNULATED SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K102903
510(k) Type
Special
Applicant
PIONEER SURGICAL TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/2010
Days to Decision
20 days
Submission Type
Summary