Last synced on 14 November 2025 at 11:06 pm

COROENT XLR STANDALONE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K100043
510(k) Type
Traditional
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/2010
Days to Decision
159 days
Submission Type
Summary

COROENT XLR STANDALONE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K100043
510(k) Type
Traditional
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/2010
Days to Decision
159 days
Submission Type
Summary