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GENESYS SPINE TILOCK SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K103671
510(k) Type
Special
Applicant
GENESYS SPINE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/2011
Days to Decision
217 days
Submission Type
Summary

GENESYS SPINE TILOCK SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K103671
510(k) Type
Special
Applicant
GENESYS SPINE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/2011
Days to Decision
217 days
Submission Type
Summary