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ORTHOPEDIC DEVICES

Page Type
Cleared 510(K)
510(k) Number
K780235
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/1978
Days to Decision
10 days

ORTHOPEDIC DEVICES

Page Type
Cleared 510(K)
510(k) Number
K780235
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/1978
Days to Decision
10 days