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LATERAL FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K112986
510(k) Type
Special
Applicant
INTEGRA SPINE (INTEGRA LIFESCIENCES)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/2012
Days to Decision
208 days
Submission Type
Summary

LATERAL FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K112986
510(k) Type
Special
Applicant
INTEGRA SPINE (INTEGRA LIFESCIENCES)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/2012
Days to Decision
208 days
Submission Type
Summary