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PRIME FEMORAL CEMENT PLUG

Page Type
Cleared 510(K)
510(k) Number
K955751
510(k) Type
Traditional
Applicant
ORTHOPAEDIC INNOVATIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1996
Days to Decision
37 days
Submission Type
Summary

PRIME FEMORAL CEMENT PLUG

Page Type
Cleared 510(K)
510(k) Number
K955751
510(k) Type
Traditional
Applicant
ORTHOPAEDIC INNOVATIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1996
Days to Decision
37 days
Submission Type
Summary