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OTI BONE CEMENT PLUG

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030608
510(k) Type
Traditional
Applicant
Osteoimplant Technology, Inc.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
6/12/2003
Days to Decision
106 days
Submission Type
Statement

OTI BONE CEMENT PLUG

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030608
510(k) Type
Traditional
Applicant
Osteoimplant Technology, Inc.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
6/12/2003
Days to Decision
106 days
Submission Type
Statement