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SEQUOIA PEDICLE SCREW SYSTEM INCLUDING SPEEDLINK II TRANSVERSE CONNECTOR SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131980
510(k) Type
Traditional
Applicant
Zimmer Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/2013
Days to Decision
68 days
Submission Type
Summary

SEQUOIA PEDICLE SCREW SYSTEM INCLUDING SPEEDLINK II TRANSVERSE CONNECTOR SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131980
510(k) Type
Traditional
Applicant
Zimmer Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/2013
Days to Decision
68 days
Submission Type
Summary