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FDA 510(k), K941691, REVO ROTATOR CUFF REPAIR SYSTEM
FDA 510(k), K941691, REVO ROTATOR CUFF REPAIR SYSTEM
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$149.00 USD
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$149.00 USD
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510(K) Number: K941691
Device Name: REVO ROTATOR CUFF REPAIR SYSTEM
Manufacturer:
Device Classification Name: Arthroscope
Regulation Number: 888.1100
Classification Product Code: HRX
Date Received: 04/06/1994
Decision Date: 09/06/1994
Regulation Medical Specialty: Orthopedic
Device Name: REVO ROTATOR CUFF REPAIR SYSTEM
Manufacturer:
Device Classification Name: Arthroscope
Regulation Number: 888.1100
Classification Product Code: HRX
Date Received: 04/06/1994
Decision Date: 09/06/1994
Regulation Medical Specialty: Orthopedic
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