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FDA 510(k), K884888, MODIFIED NEW JERSEY ACETABULAR COMP. & BONE SCREWS
FDA 510(k), K884888, MODIFIED NEW JERSEY ACETABULAR COMP. & BONE SCREWS
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510(K) Number: K884888
Device Name: MODIFIED NEW JERSEY ACETABULAR COMP. & BONE SCREWS
Manufacturer: PROTEK, INC.
Device Classification Name: prosthesis, hip, semi-constrained, metal/polymer, cemented
Regulation Number: 888.3350
Classification Product Code: JDI
Date Received: 11/22/1988
Decision Date: 12/29/1988
Regulation Medical Specialty: Orthopedic
Device Name: MODIFIED NEW JERSEY ACETABULAR COMP. & BONE SCREWS
Manufacturer: PROTEK, INC.
Device Classification Name: prosthesis, hip, semi-constrained, metal/polymer, cemented
Regulation Number: 888.3350
Classification Product Code: JDI
Date Received: 11/22/1988
Decision Date: 12/29/1988
Regulation Medical Specialty: Orthopedic
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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