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CC-Clip® Implant System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232780
510(k) Type
Traditional
Applicant
CC-Instruments Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2023
Days to Decision
98 days
Submission Type
Summary

CC-Clip® Implant System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232780
510(k) Type
Traditional
Applicant
CC-Instruments Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2023
Days to Decision
98 days
Submission Type
Summary