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FDA 510(k), K800494, NEW JERSEY HEMIARTHROPLASTY SHOLDER PROS
FDA 510(k), K800494, NEW JERSEY HEMIARTHROPLASTY SHOLDER PROS
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510(K) Number: K800494
Device Name: NEW JERSEY HEMIARTHROPLASTY SHOLDER PROS
Manufacturer: DEPUY, INC.
Device Classification Name: prosthesis, shoulder, hemi-, humeral, metallic uncemented
Regulation Number: 888.3690
Classification Product Code: HSD
Date Received: 03/04/1980
Decision Date: 03/18/1980
Regulation Medical Specialty: Orthopedic
Device Name: NEW JERSEY HEMIARTHROPLASTY SHOLDER PROS
Manufacturer: DEPUY, INC.
Device Classification Name: prosthesis, shoulder, hemi-, humeral, metallic uncemented
Regulation Number: 888.3690
Classification Product Code: HSD
Date Received: 03/04/1980
Decision Date: 03/18/1980
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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