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Twin Peaks 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
K152355
510(k) Type
Traditional
Applicant
SPINEWAY
Country
France
FDA Decision
Substantially Equivalent
Decision Date
12/10/2015
Days to Decision
112 days
Submission Type
Summary

Twin Peaks 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
K152355
510(k) Type
Traditional
Applicant
SPINEWAY
Country
France
FDA Decision
Substantially Equivalent
Decision Date
12/10/2015
Days to Decision
112 days
Submission Type
Summary