Last synced on 25 April 2025 at 11:05 pm

SEQUOIA SPINAL SYSTEM (MODEL 3306), SPEEDLINK TRANSVERSE CONNECTOR (MODELS 3308, 3309, 3310)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082032
510(k) Type
Traditional
Applicant
ABBOTT SPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/2008
Days to Decision
81 days
Submission Type
Summary

SEQUOIA SPINAL SYSTEM (MODEL 3306), SPEEDLINK TRANSVERSE CONNECTOR (MODELS 3308, 3309, 3310)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082032
510(k) Type
Traditional
Applicant
ABBOTT SPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/2008
Days to Decision
81 days
Submission Type
Summary