FDA 510(k), K033981, SMITH & NEPHEW ELECTROTHERMAL 20S SPINE GENERATOR, MODEL 7209975
FDA 510(k), K033981, SMITH & NEPHEW ELECTROTHERMAL 20S SPINE GENERATOR, MODEL 7209975
Device Name: SMITH & NEPHEW ELECTROTHERMAL 20S SPINE GENERATOR, MODEL 7209975
Manufacturer:
Device Classification Name: Electrosurgical, Cutting & Coagulation & Accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 12/23/2003
Decision Date: 02/25/2004
Regulation Medical Specialty: General & Plastic Surgery
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