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Arthrex UNIVERS REVERS COATED BASEPLATE

Page Type
Cleared 510(K)
510(k) Number
K172371
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2018
Days to Decision
227 days
Submission Type
Summary

Arthrex UNIVERS REVERS COATED BASEPLATE

Page Type
Cleared 510(K)
510(k) Number
K172371
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2018
Days to Decision
227 days
Submission Type
Summary