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SPINESMITH PARTNERS, LP CEQUENCE ANTERIOR CERVICAL PLATE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081132
510(k) Type
Traditional
Applicant
SPINE SMITH PARTNERS L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/2008
Days to Decision
84 days
Submission Type
Summary

SPINESMITH PARTNERS, LP CEQUENCE ANTERIOR CERVICAL PLATE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081132
510(k) Type
Traditional
Applicant
SPINE SMITH PARTNERS L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/2008
Days to Decision
84 days
Submission Type
Summary