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Summit Spine Yellowstone Lumbar Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K170572
510(k) Type
Traditional
Applicant
Summit Spine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/2017
Days to Decision
58 days
Submission Type
Summary

Summit Spine Yellowstone Lumbar Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K170572
510(k) Type
Traditional
Applicant
Summit Spine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/2017
Days to Decision
58 days
Submission Type
Summary