Last synced on 18 April 2025 at 11:05 pm

PRO OSTEON 200R RESORBABLE BONE GRAFT SUBSTITUTE, MODELS 2RG051, 2RG101, 2RG151, 2RG201, 2RG301, 2RG050, 2RG100, 2RG150,

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000515
510(k) Type
Traditional
Applicant
INTERPORE CROSS INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/2000
Days to Decision
212 days
Submission Type
Summary

PRO OSTEON 200R RESORBABLE BONE GRAFT SUBSTITUTE, MODELS 2RG051, 2RG101, 2RG151, 2RG201, 2RG301, 2RG050, 2RG100, 2RG150,

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000515
510(k) Type
Traditional
Applicant
INTERPORE CROSS INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/2000
Days to Decision
212 days
Submission Type
Summary