Last synced on 1 March 2024 at 11:05 pm

MD Mattress Suture Placement Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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