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TunneLoc Tibial Fixation Device

Page Type
Cleared 510(K)
510(k) Number
K193092
510(k) Type
Traditional
Applicant
Biomet Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/2/2020
Days to Decision
57 days
Submission Type
Summary

TunneLoc Tibial Fixation Device

Page Type
Cleared 510(K)
510(k) Number
K193092
510(k) Type
Traditional
Applicant
Biomet Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/2/2020
Days to Decision
57 days
Submission Type
Summary