Last synced on 25 January 2026 at 3:41 am

icotec Interbody Cage System (icotec Cervical Cage, icotec PLIF Lumbar Cage, icotec ETurn™ TLIF Lumbar Cage)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232792
510(k) Type
Traditional
Applicant
Icotec AG
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
4/5/2024
Days to Decision
207 days
Submission Type
Summary

icotec Interbody Cage System (icotec Cervical Cage, icotec PLIF Lumbar Cage, icotec ETurn™ TLIF Lumbar Cage)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232792
510(k) Type
Traditional
Applicant
Icotec AG
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
4/5/2024
Days to Decision
207 days
Submission Type
Summary