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FDA 510(k), K051843, COPELAND EAS HUMERAL RESURFACING HEADS
FDA 510(k), K051843, COPELAND EAS HUMERAL RESURFACING HEADS
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510(K) Number: K051843
Device Name: COPELAND EAS HUMERAL RESURFACING HEADS
Manufacturer: BIOMET, INC.
Device Classification Name: Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented
Regulation Number: 888.3690
Classification Product Code: HSD
Date Received: 07/07/2005
Decision Date: 09/29/2005
Regulation Medical Specialty: Orthopedic
Total Pages: 164
Fully Redacted Pages: 105
Content Pages: 59
Device Name: COPELAND EAS HUMERAL RESURFACING HEADS
Manufacturer: BIOMET, INC.
Device Classification Name: Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented
Regulation Number: 888.3690
Classification Product Code: HSD
Date Received: 07/07/2005
Decision Date: 09/29/2005
Regulation Medical Specialty: Orthopedic
Total Pages: 164
Fully Redacted Pages: 105
Content Pages: 59
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