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FLXFIT INTERVERTEBRAL BODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K133813
510(k) Type
Traditional
Applicant
EXPANDING ORTHOPEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/2014
Days to Decision
211 days
Submission Type
Summary

FLXFIT INTERVERTEBRAL BODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K133813
510(k) Type
Traditional
Applicant
EXPANDING ORTHOPEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/2014
Days to Decision
211 days
Submission Type
Summary