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Resorbable Mesh Device

Page Type
Cleared 510(K)
510(k) Number
K193040
510(k) Type
Special
Applicant
SeaSpine Orthopedics Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/30/2019
Days to Decision
30 days
Submission Type
Summary

Resorbable Mesh Device

Page Type
Cleared 510(K)
510(k) Number
K193040
510(k) Type
Special
Applicant
SeaSpine Orthopedics Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/30/2019
Days to Decision
30 days
Submission Type
Summary