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CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments; CarboClear® X Fenestrated Pedicle Screw System with 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
K231280
510(k) Type
Traditional
Applicant
Carbofix Orthopedics Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
7/3/2023
Days to Decision
61 days
Submission Type
Summary

CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments; CarboClear® X Fenestrated Pedicle Screw System with 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
K231280
510(k) Type
Traditional
Applicant
Carbofix Orthopedics Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
7/3/2023
Days to Decision
61 days
Submission Type
Summary