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FDA 510(k), K802123, MONOSPHERICAL SHOULDER PROSTHESIS
FDA 510(k), K802123, MONOSPHERICAL SHOULDER PROSTHESIS
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510(K) Number: K802123
Device Name: MONOSPHERICAL SHOULDER PROSTHESIS
Manufacturer: HOWMEDICA CORP.
Device Classification Name: prosthesis, shoulder, hemi-, humeral, metallic uncemented
Regulation Number: 888.3690
Classification Product Code: HSD
Date Received: 09/04/1980
Decision Date: 09/16/1980
Regulation Medical Specialty: Orthopedic
Device Name: MONOSPHERICAL SHOULDER PROSTHESIS
Manufacturer: HOWMEDICA CORP.
Device Classification Name: prosthesis, shoulder, hemi-, humeral, metallic uncemented
Regulation Number: 888.3690
Classification Product Code: HSD
Date Received: 09/04/1980
Decision Date: 09/16/1980
Regulation Medical Specialty: Orthopedic
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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