Last synced on 25 April 2025 at 11:05 pm

Summit Spine Yellowstone Lumbar Interbody Fusion System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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