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XTEND-ST NUCLEUS REMOVAL SYSTEM, MODEL 9004

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090303
510(k) Type
Traditional
Applicant
Corespine Technologies, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/2009
Days to Decision
83 days
Submission Type
Summary

XTEND-ST NUCLEUS REMOVAL SYSTEM, MODEL 9004

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090303
510(k) Type
Traditional
Applicant
Corespine Technologies, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/2009
Days to Decision
83 days
Submission Type
Summary