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LDR SPINE USA SPINE TUNE, TL SPINAL SYSTEM, LDR SPINE USA EASYSPINE, POSTERIOR SPINAL SYSTEM, LDR SPINE USA MC IMPLANT S

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121103
510(k) Type
Traditional
Applicant
LDR SPINE USA INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/2012
Days to Decision
135 days
Submission Type
Summary

LDR SPINE USA SPINE TUNE, TL SPINAL SYSTEM, LDR SPINE USA EASYSPINE, POSTERIOR SPINAL SYSTEM, LDR SPINE USA MC IMPLANT S

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121103
510(k) Type
Traditional
Applicant
LDR SPINE USA INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/2012
Days to Decision
135 days
Submission Type
Summary