Last synced on 14 November 2025 at 11:06 pm

EXPANSE VERTEBRAL BODY REPLACEMENT DEVICE

Page Type
Cleared 510(K)
510(k) Number
K050997
510(k) Type
Traditional
Applicant
Flexuspine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/2005
Days to Decision
170 days
Submission Type
Summary

EXPANSE VERTEBRAL BODY REPLACEMENT DEVICE

Page Type
Cleared 510(K)
510(k) Number
K050997
510(k) Type
Traditional
Applicant
Flexuspine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/2005
Days to Decision
170 days
Submission Type
Summary