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PIVOTEC LUMBAR INTERBODY FUSION DEVICE (LIFD)

Page Type
Cleared 510(K)
510(k) Number
K092017
510(k) Type
Traditional
Applicant
CAPTIVA SPINE, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/2009
Days to Decision
148 days
Submission Type
Summary

PIVOTEC LUMBAR INTERBODY FUSION DEVICE (LIFD)

Page Type
Cleared 510(K)
510(k) Number
K092017
510(k) Type
Traditional
Applicant
CAPTIVA SPINE, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/2009
Days to Decision
148 days
Submission Type
Summary