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VeriFixx™ Small Bone Implant

Page Type
Cleared 510(K)
510(k) Number
K202777
510(k) Type
Traditional
Applicant
Armis Biopharma, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2020
Days to Decision
56 days
Submission Type
Summary

VeriFixx™ Small Bone Implant

Page Type
Cleared 510(K)
510(k) Number
K202777
510(k) Type
Traditional
Applicant
Armis Biopharma, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2020
Days to Decision
56 days
Submission Type
Summary