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ACCULIF CAGE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110270
510(k) Type
Special
Applicant
Coalign Innovations, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/2011
Days to Decision
66 days
Submission Type
Summary

ACCULIF CAGE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110270
510(k) Type
Special
Applicant
Coalign Innovations, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/2011
Days to Decision
66 days
Submission Type
Summary