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InFill® Interbody Fusion Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172349
510(k) Type
Traditional
Applicant
Pinnacle Spine Group, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2017
Days to Decision
133 days
Submission Type
Summary

InFill® Interbody Fusion Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172349
510(k) Type
Traditional
Applicant
Pinnacle Spine Group, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2017
Days to Decision
133 days
Submission Type
Summary