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KLS Martin Pure Pectus System

Page Type
Cleared 510(K)
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)
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