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ANCHORMAN Tibial Ligament Fixation Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170388
510(k) Type
Traditional
Applicant
Summit Medical Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
7/25/2017
Days to Decision
167 days
Submission Type
Summary

ANCHORMAN Tibial Ligament Fixation Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170388
510(k) Type
Traditional
Applicant
Summit Medical Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
7/25/2017
Days to Decision
167 days
Submission Type
Summary