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GENESYS SPINE APACHE LATERAL LUMBAR INTERBODY FUSION SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130913
510(k) Type
Special
Applicant
Genesys Spine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2013
Days to Decision
255 days
Submission Type
Summary

GENESYS SPINE APACHE LATERAL LUMBAR INTERBODY FUSION SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130913
510(k) Type
Special
Applicant
Genesys Spine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2013
Days to Decision
255 days
Submission Type
Summary