Last synced on 23 September 2022 at 11:05 pm

NovoStitch Pro Meniscal Repair System, CTX-A004 (size 0)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181772
510(k) Type
Special
Applicant
Ceterix Orthopaedics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2018
Days to Decision
29 days
Submission Type
Summary

NovoStitch Pro Meniscal Repair System, CTX-A004 (size 0)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181772
510(k) Type
Special
Applicant
Ceterix Orthopaedics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2018
Days to Decision
29 days
Submission Type
Summary