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FUSON BONE PLUG, RADIOPAQUE

Page Type
Cleared 510(K)
510(k) Number
K800142
510(k) Type
Traditional
Applicant
ZIMMER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/1980
Days to Decision
29 days

FUSON BONE PLUG, RADIOPAQUE

Page Type
Cleared 510(K)
510(k) Number
K800142
510(k) Type
Traditional
Applicant
ZIMMER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/1980
Days to Decision
29 days