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FDA 510(k), K883969, UNI-KNEE COMPONENT OF THE NATURAL-KNEE SYSTEM
FDA 510(k), K883969, UNI-KNEE COMPONENT OF THE NATURAL-KNEE SYSTEM
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510(K) Number: K883969
Device Name: UNI-KNEE COMPONENT OF THE NATURAL-KNEE SYSTEM
Manufacturer: INTERMEDICS ORTHOPEDICS
Device Classification Name: prosthesis, knee, femorotibial, semi-constrained, cemented, metal/polymer
Regulation Number: 888.3530
Classification Product Code: HRY
Date Received: 09/20/1988
Decision Date: 04/19/1989
Regulation Medical Specialty: Orthopedic
Device Name: UNI-KNEE COMPONENT OF THE NATURAL-KNEE SYSTEM
Manufacturer: INTERMEDICS ORTHOPEDICS
Device Classification Name: prosthesis, knee, femorotibial, semi-constrained, cemented, metal/polymer
Regulation Number: 888.3530
Classification Product Code: HRY
Date Received: 09/20/1988
Decision Date: 04/19/1989
Regulation Medical Specialty: Orthopedic
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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