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MICRORAPTOR REGENESORB Suture Anchor

Page Type
Cleared 510(K)
510(k) Number
K180361
510(k) Type
Traditional
Applicant
Smith and Nephew, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/2018
Days to Decision
110 days
Submission Type
Summary

MICRORAPTOR REGENESORB Suture Anchor

Page Type
Cleared 510(K)
510(k) Number
K180361
510(k) Type
Traditional
Applicant
Smith and Nephew, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/2018
Days to Decision
110 days
Submission Type
Summary