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Interphalangeal Joint Fusion Device Range

Page Type
Cleared 510(K)
510(k) Number
K191424
510(k) Type
Traditional
Applicant
Neosteo
Country
France
FDA Decision
Substantially Equivalent
Decision Date
8/28/2019
Days to Decision
91 days
Submission Type
Summary

Interphalangeal Joint Fusion Device Range

Page Type
Cleared 510(K)
510(k) Number
K191424
510(k) Type
Traditional
Applicant
Neosteo
Country
France
FDA Decision
Substantially Equivalent
Decision Date
8/28/2019
Days to Decision
91 days
Submission Type
Summary