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APOLLO ANTERIOR CERVICAL PLATE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082504
510(k) Type
Traditional
Applicant
APOLLO SPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/2009
Days to Decision
151 days
Submission Type
Summary

APOLLO ANTERIOR CERVICAL PLATE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082504
510(k) Type
Traditional
Applicant
APOLLO SPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/2009
Days to Decision
151 days
Submission Type
Summary