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EIT Cellular Titanium® Lumbar Cage LLIF

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181644
510(k) Type
Traditional
Applicant
EIT Emerging Implant Technologies GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
10/12/2018
Days to Decision
112 days
Submission Type
Summary

EIT Cellular Titanium® Lumbar Cage LLIF

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181644
510(k) Type
Traditional
Applicant
EIT Emerging Implant Technologies GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
10/12/2018
Days to Decision
112 days
Submission Type
Summary