Last synced on 18 April 2025 at 11:05 pm

PRO OSTEON IMPLANT 500R RESORBABLE BONE GRAFT SUBSTITUTE MODEL NUMBERS 5RG05, 5RG10, 5RG15, 5G15L, 5RG20, 5RG30, 5RG30L

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980817
510(k) Type
Traditional
Applicant
INTERPORE INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/1998
Days to Decision
206 days
Submission Type
Summary

PRO OSTEON IMPLANT 500R RESORBABLE BONE GRAFT SUBSTITUTE MODEL NUMBERS 5RG05, 5RG10, 5RG15, 5G15L, 5RG20, 5RG30, 5RG30L

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980817
510(k) Type
Traditional
Applicant
INTERPORE INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/1998
Days to Decision
206 days
Submission Type
Summary