Last synced on 9 May 2025 at 11:05 pm

VLIFT-S VERTEBRAL BODY REPLACEMENT SYSTEM, MODELS 488812XX, 488814XX, 488816XX, 488818XX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091946
510(k) Type
Traditional
Applicant
STRYKER SPINE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/2009
Days to Decision
87 days
Submission Type
Summary

VLIFT-S VERTEBRAL BODY REPLACEMENT SYSTEM, MODELS 488812XX, 488814XX, 488816XX, 488818XX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091946
510(k) Type
Traditional
Applicant
STRYKER SPINE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/2009
Days to Decision
87 days
Submission Type
Summary