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Resorbable Mesh Device

Page Type
Cleared 510(K)
510(k) Number
K172130
510(k) Type
Traditional
Applicant
SeaSpine Orthopedics Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2017
Days to Decision
125 days
Submission Type
Summary

Resorbable Mesh Device

Page Type
Cleared 510(K)
510(k) Number
K172130
510(k) Type
Traditional
Applicant
SeaSpine Orthopedics Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2017
Days to Decision
125 days
Submission Type
Summary