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NeoSpan® Compression Implant System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233089
510(k) Type
Traditional
Applicant
In2bones USA, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/24/2024
Days to Decision
241 days
Submission Type
Summary

NeoSpan® Compression Implant System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233089
510(k) Type
Traditional
Applicant
In2bones USA, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/24/2024
Days to Decision
241 days
Submission Type
Summary