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Integrity Spine Lumbar Interbody Fusion System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151819
510(k) Type
Traditional
Applicant
INTEGRITY SPINE LUMBAR INTERBODY FUSION SYSTEM
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/10/2015
Days to Decision
127 days
Submission Type
Summary

Integrity Spine Lumbar Interbody Fusion System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151819
510(k) Type
Traditional
Applicant
INTEGRITY SPINE LUMBAR INTERBODY FUSION SYSTEM
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/10/2015
Days to Decision
127 days
Submission Type
Summary