Last synced on 25 January 2026 at 3:41 am

Guided Surgery Kit

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231087
510(k) Type
Traditional
Applicant
Implant Direct Sybron Manufacturing, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/2023
Days to Decision
121 days
Submission Type
Summary

Guided Surgery Kit

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231087
510(k) Type
Traditional
Applicant
Implant Direct Sybron Manufacturing, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/2023
Days to Decision
121 days
Submission Type
Summary