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FDA 510(k), K002149, LINEAGE ACETABULAR SYSTEM
FDA 510(k), K002149, LINEAGE ACETABULAR SYSTEM
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510(K) Number: K002149
Device Name: LINEAGE ACETABULAR SYSTEM
Manufacturer: WRIGHT MEDICAL TECHNOLOGY, INC.
Device Classification Name: prosthesis, hip, semi-constrained, metal/polymer, porous uncemented
Regulation Number: 888.3358
Classification Product Code: LPH
Date Received: 07/17/2000
Decision Date: 08/31/2000
Regulation Medical Specialty: Orthopedic
Device Name: LINEAGE ACETABULAR SYSTEM
Manufacturer: WRIGHT MEDICAL TECHNOLOGY, INC.
Device Classification Name: prosthesis, hip, semi-constrained, metal/polymer, porous uncemented
Regulation Number: 888.3358
Classification Product Code: LPH
Date Received: 07/17/2000
Decision Date: 08/31/2000
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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