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AccuLIF TL and PL Cage

Page Type
Cleared 510(K)
510(k) Number
K152651
510(k) Type
Traditional
Applicant
STRYKER CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/15/2015
Days to Decision
90 days
Submission Type
Summary

AccuLIF TL and PL Cage

Page Type
Cleared 510(K)
510(k) Number
K152651
510(k) Type
Traditional
Applicant
STRYKER CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/15/2015
Days to Decision
90 days
Submission Type
Summary