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Camber Sacroiliac (SI) Fixation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233972
510(k) Type
Traditional
Applicant
Camber Spine Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/2024
Days to Decision
74 days
Submission Type
Summary

Camber Sacroiliac (SI) Fixation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233972
510(k) Type
Traditional
Applicant
Camber Spine Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/2024
Days to Decision
74 days
Submission Type
Summary