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PIONEER INTERVERTEBRAL FUSION DEVICE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K073177
510(k) Type
Abbreviated
Applicant
PIONEER SURGICAL TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/2008
Days to Decision
182 days
Submission Type
Summary

PIONEER INTERVERTEBRAL FUSION DEVICE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K073177
510(k) Type
Abbreviated
Applicant
PIONEER SURGICAL TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/2008
Days to Decision
182 days
Submission Type
Summary