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LANX CERVICAL INTERVERTEBRAL BODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K082774
510(k) Type
Traditional
Applicant
LANX, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/2008
Days to Decision
29 days
Submission Type
Summary

LANX CERVICAL INTERVERTEBRAL BODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K082774
510(k) Type
Traditional
Applicant
LANX, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/2008
Days to Decision
29 days
Submission Type
Summary