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MODIFICATION TO EBI SPINELINK SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003764
510(k) Type
Special
Applicant
Ebi, L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/2/2001
Days to Decision
27 days
Submission Type
Summary

MODIFICATION TO EBI SPINELINK SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003764
510(k) Type
Special
Applicant
Ebi, L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/2/2001
Days to Decision
27 days
Submission Type
Summary