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SPIRA® Posterior Lumbar Spacers

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230942
510(k) Type
Traditional
Applicant
Camber Spine Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/11/2023
Days to Decision
99 days
Submission Type
Summary

SPIRA® Posterior Lumbar Spacers

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230942
510(k) Type
Traditional
Applicant
Camber Spine Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/11/2023
Days to Decision
99 days
Submission Type
Summary