Last synced on 24 May 2024 at 11:04 pm

Patient Contoured Implant-PEEK (PCI-PEEK)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151382
510(k) Type
Traditional
Applicant
KLS MARTIN L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/2015
Days to Decision
171 days
Submission Type
Summary

Patient Contoured Implant-PEEK (PCI-PEEK)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151382
510(k) Type
Traditional
Applicant
KLS MARTIN L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/2015
Days to Decision
171 days
Submission Type
Summary