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Camber Sacroiliac (SI) Fixation System

Page Type
Cleared 510(K)
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)
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