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MODIFICATION TO LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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