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OSTEOGEN (HA RESORB)

Page Type
Cleared 510(K)
510(k) Number
K923310
510(k) Type
Traditional
Applicant
IMPLADENT
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/1995
Days to Decision
1058 days
Submission Type
Statement

OSTEOGEN (HA RESORB)

Page Type
Cleared 510(K)
510(k) Number
K923310
510(k) Type
Traditional
Applicant
IMPLADENT
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/1995
Days to Decision
1058 days
Submission Type
Statement