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S-LIF INTERVERTEBRAL BODY FUSION DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092815
510(k) Type
Abbreviated
Applicant
Spinefrontier, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/2010
Days to Decision
289 days
Submission Type
Summary

S-LIF INTERVERTEBRAL BODY FUSION DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092815
510(k) Type
Abbreviated
Applicant
Spinefrontier, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/2010
Days to Decision
289 days
Submission Type
Summary