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LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K092656
510(k) Type
Traditional
Applicant
LANX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/24/2009
Days to Decision
88 days
Submission Type
Summary

LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K092656
510(k) Type
Traditional
Applicant
LANX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/24/2009
Days to Decision
88 days
Submission Type
Summary