Last synced on 9 December 2022 at 11:04 pm

CREODENT SOLIDEX CUSTOM ABUTMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K113738
510(k) Type
Traditional
Applicant
CREODENT PROSTHETICS LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/2013
Days to Decision
637 days
Submission Type
Summary

CREODENT SOLIDEX CUSTOM ABUTMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K113738
510(k) Type
Traditional
Applicant
CREODENT PROSTHETICS LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/2013
Days to Decision
637 days
Submission Type
Summary