Last synced on 25 April 2025 at 11:05 pm

CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233944
510(k) Type
Special
Applicant
CarboFix Orthopedics, Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
1/10/2024
Days to Decision
27 days
Submission Type
Summary

CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233944
510(k) Type
Special
Applicant
CarboFix Orthopedics, Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
1/10/2024
Days to Decision
27 days
Submission Type
Summary