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GENESYS SPINE TILOCK SYSTEM

Page Type
Cleared 510(K)
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)
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