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JuggerStitch Meniscal Repair Device

Page Type
Cleared 510(K)
510(k) Number
K191459
510(k) Type
Traditional
Applicant
Biomet Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/2019
Days to Decision
102 days
Submission Type
Summary

JuggerStitch Meniscal Repair Device

Page Type
Cleared 510(K)
510(k) Number
K191459
510(k) Type
Traditional
Applicant
Biomet Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/2019
Days to Decision
102 days
Submission Type
Summary