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KELYNIAM CUSTOM SKULL IMPLANT (CSI)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K103582
510(k) Type
Traditional
Applicant
Kelyniam Global, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/14/2011
Days to Decision
127 days
Submission Type
Summary

KELYNIAM CUSTOM SKULL IMPLANT (CSI)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K103582
510(k) Type
Traditional
Applicant
Kelyniam Global, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/14/2011
Days to Decision
127 days
Submission Type
Summary