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TiLock2 Spinal System

Page Type
Cleared 510(K)
510(k) Number
K171838
510(k) Type
Special
Applicant
Genesys Spine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2017
Days to Decision
29 days
Submission Type
Summary

TiLock2 Spinal System

Page Type
Cleared 510(K)
510(k) Number
K171838
510(k) Type
Special
Applicant
Genesys Spine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2017
Days to Decision
29 days
Submission Type
Summary