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Spinal Jaxx Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K152501
510(k) Type
Traditional
Applicant
NEUROPRO SPINAL JAXX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/29/2016
Days to Decision
302 days
Submission Type
Summary

Spinal Jaxx Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K152501
510(k) Type
Traditional
Applicant
NEUROPRO SPINAL JAXX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/29/2016
Days to Decision
302 days
Submission Type
Summary