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CONDUIT™ Lateral Lumbar Intervertebral Fusion Cage, CONDUIT™ Instruments

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223688
510(k) Type
Traditional
Applicant
Medos International SÀRL
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
3/8/2023
Days to Decision
89 days
Submission Type
Summary

CONDUIT™ Lateral Lumbar Intervertebral Fusion Cage, CONDUIT™ Instruments

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223688
510(k) Type
Traditional
Applicant
Medos International SÀRL
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
3/8/2023
Days to Decision
89 days
Submission Type
Summary