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LINK® BiMobile(TM) Dual Mobility System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171273
510(k) Type
Traditional
Applicant
Waldemar Link GmbH & Co. KG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
1/19/2018
Days to Decision
263 days
Submission Type
Summary

LINK® BiMobile(TM) Dual Mobility System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171273
510(k) Type
Traditional
Applicant
Waldemar Link GmbH & Co. KG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
1/19/2018
Days to Decision
263 days
Submission Type
Summary