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KLS Martin Pure Pectus System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221938
510(k) Type
Traditional
Applicant
KLS Martin L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2023
Days to Decision
270 days
Submission Type
Summary

KLS Martin Pure Pectus System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221938
510(k) Type
Traditional
Applicant
KLS Martin L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2023
Days to Decision
270 days
Submission Type
Summary