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MD Mattress Suture Placement Device

Page Type
Cleared 510(K)
510(k) Number
K222783
510(k) Type
Traditional
Applicant
Lsi Solutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2024
Days to Decision
484 days
Submission Type
Summary

MD Mattress Suture Placement Device

Page Type
Cleared 510(K)
510(k) Number
K222783
510(k) Type
Traditional
Applicant
Lsi Solutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2024
Days to Decision
484 days
Submission Type
Summary