Last synced on 18 April 2025 at 11:05 pm

NeoSpan® Compression Implant System

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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