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DIAMOND ANTERIOR CERVICAL PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K100265
510(k) Type
Traditional
Applicant
AMENDIA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/2010
Days to Decision
104 days
Submission Type
Summary

DIAMOND ANTERIOR CERVICAL PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K100265
510(k) Type
Traditional
Applicant
AMENDIA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/2010
Days to Decision
104 days
Submission Type
Summary