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FaSet Fixation System, UNITY Sacroiliac Joint Fixation System, Huvex Interspinous Fixation System, and AEON-C™ Stand Alone System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232877
510(k) Type
Traditional
Applicant
K&J Consulting Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2023
Days to Decision
89 days
Submission Type
Summary

FaSet Fixation System, UNITY Sacroiliac Joint Fixation System, Huvex Interspinous Fixation System, and AEON-C™ Stand Alone System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232877
510(k) Type
Traditional
Applicant
K&J Consulting Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2023
Days to Decision
89 days
Submission Type
Summary