OTI BONE CEMENT PLUG— 510(k) K030608

Unknown

Osteoimplant Technology, Inc.

FDA 510(k) clearance K030608 for OTI BONE CEMENT PLUG, Unknown on 2003-06-12. Applicant: Osteoimplant Technology, Inc.. Device class: 2.

Clearance details

Applicant: Osteoimplant Technology, Inc.
Product code: Code JDK
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 2003-02-26
Decision date: 2003-06-12
Decision: Unknown
Clearance type: Traditional
Location: Hunt Valley, MD, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.