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FDA 510(k), K110895, ORTHO SOLUTIONS TRAUMA IMPLANTS FOR OSTEOSYNTHESIS
FDA 510(k), K110895, ORTHO SOLUTIONS TRAUMA IMPLANTS FOR OSTEOSYNTHESIS
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510(K) Number: K110895
Device Name: ORTHO SOLUTIONS TRAUMA IMPLANTS FOR OSTEOSYNTHESIS
Manufacturer: ORTHO SOLUTIONS LIMITED
Device Classification Name: screw, fixation, bone
Regulation Number: 888.3040
Classification Product Code: HWC
Date Received: 03/30/2011
Decision Date: 12/19/2011
Regulation Medical Specialty: Orthopedic
Device Name: ORTHO SOLUTIONS TRAUMA IMPLANTS FOR OSTEOSYNTHESIS
Manufacturer: ORTHO SOLUTIONS LIMITED
Device Classification Name: screw, fixation, bone
Regulation Number: 888.3040
Classification Product Code: HWC
Date Received: 03/30/2011
Decision Date: 12/19/2011
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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