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ACCULIF TL-PEEK CAGE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123281
510(k) Type
Traditional
Applicant
Coalign Innovations, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/2013
Days to Decision
93 days
Submission Type
Summary

ACCULIF TL-PEEK CAGE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123281
510(k) Type
Traditional
Applicant
Coalign Innovations, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/2013
Days to Decision
93 days
Submission Type
Summary