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FDA 510(k), K894184, BIEDERMANN MOTECH UNIVERSAL SPINAL SYSTEM
FDA 510(k), K894184, BIEDERMANN MOTECH UNIVERSAL SPINAL SYSTEM
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510(K) Number: K894184
Device Name: BIEDERMANN MOTECH UNIVERSAL SPINAL SYSTEM
Manufacturer: BIEDERMANN MOTECH GMBH
Device Classification Name: implant, fixation device, spinal
Regulation Number: 888.3060
Classification Product Code: JDN
Date Received: 06/16/1989
Decision Date: 04/25/1990
Regulation Medical Specialty: Orthopedic
Device Name: BIEDERMANN MOTECH UNIVERSAL SPINAL SYSTEM
Manufacturer: BIEDERMANN MOTECH GMBH
Device Classification Name: implant, fixation device, spinal
Regulation Number: 888.3060
Classification Product Code: JDN
Date Received: 06/16/1989
Decision Date: 04/25/1990
Regulation Medical Specialty: Orthopedic
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- Delivery: Approximately 1 to 2 weeks
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