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SPINEFRONTIER A-CIFT SOLOFUSE CERVICAL INTERVERTEBRAL FUSION DEVICE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K131880
510(k) Type
Abbreviated
Applicant
SPINEFRONTIER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/2014
Days to Decision
192 days
Submission Type
Summary

SPINEFRONTIER A-CIFT SOLOFUSE CERVICAL INTERVERTEBRAL FUSION DEVICE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K131880
510(k) Type
Abbreviated
Applicant
SPINEFRONTIER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/2014
Days to Decision
192 days
Submission Type
Summary