Last synced on 25 April 2025 at 11:05 pm

CarboClear® Hybrid Pedicle Screw System; CarboClear® Hybrid Navigated Instruments; CarboClear® Hybrid Fenestrated Pedicle Screw System and High V+® Bone Cement; CarboClear® X Fenestrated Pedicle Screw System and High V+® Bone Cement

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240846
510(k) Type
Special
Applicant
CarboFix Orthopedics Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
4/25/2024
Days to Decision
29 days
Submission Type
Summary

CarboClear® Hybrid Pedicle Screw System; CarboClear® Hybrid Navigated Instruments; CarboClear® Hybrid Fenestrated Pedicle Screw System and High V+® Bone Cement; CarboClear® X Fenestrated Pedicle Screw System and High V+® Bone Cement

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240846
510(k) Type
Special
Applicant
CarboFix Orthopedics Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
4/25/2024
Days to Decision
29 days
Submission Type
Summary