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ACCULIF TL AND PL CAGE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141217
510(k) Type
Special
Applicant
Stryker Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/2014
Days to Decision
65 days
Submission Type
Summary

ACCULIF TL AND PL CAGE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141217
510(k) Type
Special
Applicant
Stryker Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/2014
Days to Decision
65 days
Submission Type
Summary