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FDA 510(k), K170359, Trinity™ Dual Mobility System
FDA 510(k), K170359, Trinity™ Dual Mobility System
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510(K) Number: K170359
Device Name: Trinity™ Dual Mobility System
Manufacturer: Corin USA Limited
Device Classification Name: prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented
Regulation Number: 888.3353
Classification Product Code: LZO
Date Received: 02/06/2017
Decision Date: 10/31/2017
Regulation Medical Specialty: Orthopedic
Device Name: Trinity™ Dual Mobility System
Manufacturer: Corin USA Limited
Device Classification Name: prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented
Regulation Number: 888.3353
Classification Product Code: LZO
Date Received: 02/06/2017
Decision Date: 10/31/2017
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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