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TITANIUM IMPLANT DEVICES

Page Type
Cleared 510(K)
510(k) Number
K820013
510(k) Type
Traditional
Applicant
BOFORS NOBELPHARMA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/1982
Days to Decision
55 days

TITANIUM IMPLANT DEVICES

Page Type
Cleared 510(K)
510(k) Number
K820013
510(k) Type
Traditional
Applicant
BOFORS NOBELPHARMA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/1982
Days to Decision
55 days