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SPINERX-LDM

Page Type
Cleared 510(K)
510(k) Number
K031862
510(k) Type
Traditional
Applicant
SPINERX TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/2003
Days to Decision
137 days
Submission Type
Summary

SPINERX-LDM

Page Type
Cleared 510(K)
510(k) Number
K031862
510(k) Type
Traditional
Applicant
SPINERX TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/2003
Days to Decision
137 days
Submission Type
Summary