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LEVA (TM) SPACER SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141980
510(k) Type
Traditional
Applicant
Spine Wave, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/2015
Days to Decision
189 days
Submission Type
Summary

LEVA (TM) SPACER SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141980
510(k) Type
Traditional
Applicant
Spine Wave, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/2015
Days to Decision
189 days
Submission Type
Summary