OMNIPLASTIC BONE CEMENT

FDA Premarket Approval N17113

Pre-market Approval Supplement Details

• Device: OMNIPLASTIC BONE CEMENT
• Generic Name: Bone Cement
• Applicant: L.D. CAULK CO.
• Date Received: 1981-02-27
• Decision Date: 1981-09-16
• Notice Date: 1981-12-04
• PMA: N17113
• Supplement: S
• Product Code: LOD
• Docket Number: 81M-0308
• Advisory Committee: Orthopedic
• Expedited Review: No
• Combination Product: No
• Applicant Address: L.D. CAULK CO. lakeview & Clarke Avenues milford, DE 19963

Supplemental Filings

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Supplement Number	Date	Supplement Type
N17113		Original Filing