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OSTEOGEN (HA RESORB)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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