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MODIFICATION TO: VENTED CEMENT RESTRICTOR, MODEL 60102-000-001/004

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050699
510(k) Type
Special
Applicant
AMEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/2005
Days to Decision
28 days
Submission Type
Summary

MODIFICATION TO: VENTED CEMENT RESTRICTOR, MODEL 60102-000-001/004

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050699
510(k) Type
Special
Applicant
AMEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/2005
Days to Decision
28 days
Submission Type
Summary