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MODIFICATION TO LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K100888
510(k) Type
Special
Applicant
LANX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2010
Days to Decision
230 days
Submission Type
Summary

MODIFICATION TO LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K100888
510(k) Type
Special
Applicant
LANX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2010
Days to Decision
230 days
Submission Type
Summary