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Triton™ Sacroiliac Joint Fixation System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211449
510(k) Type
Traditional
Applicant
Choice Spine, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/31/2021
Days to Decision
113 days
Submission Type
Summary

Triton™ Sacroiliac Joint Fixation System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211449
510(k) Type
Traditional
Applicant
Choice Spine, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/31/2021
Days to Decision
113 days
Submission Type
Summary