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SEEPLATE CERVICAL PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K082037
510(k) Type
Special
Applicant
AMEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/2008
Days to Decision
71 days
Submission Type
Summary

SEEPLATE CERVICAL PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K082037
510(k) Type
Special
Applicant
AMEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/2008
Days to Decision
71 days
Submission Type
Summary