Last synced on 14 November 2025 at 11:06 pm

DURACON INSET PATELLA WITH CENTRAL PEG

Page Type
Cleared 510(K)
510(k) Number
K961482
510(k) Type
Traditional
Applicant
HOWMEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/5/1996
Days to Decision
78 days
Submission Type
Summary

DURACON INSET PATELLA WITH CENTRAL PEG

Page Type
Cleared 510(K)
510(k) Number
K961482
510(k) Type
Traditional
Applicant
HOWMEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/5/1996
Days to Decision
78 days
Submission Type
Summary