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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
FDA Hosted 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
FDA Hosted 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