Last synced on 25 January 2026 at 3:41 am

NEXGEN PRIMARY POROUS PATELLA, MODEL 04-211-IIII-5878-65-ZZ-(STANDARD),04-212-IIII-5878-61-ZZ-(MICRO)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011904
510(k) Type
Special
Applicant
Implex Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2001
Days to Decision
30 days
Submission Type
Summary

NEXGEN PRIMARY POROUS PATELLA, MODEL 04-211-IIII-5878-65-ZZ-(STANDARD),04-212-IIII-5878-61-ZZ-(MICRO)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011904
510(k) Type
Special
Applicant
Implex Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2001
Days to Decision
30 days
Submission Type
Summary