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FDA 510(k), K120486, AVS AS PEEK SPACER
FDA 510(k), K120486, AVS AS PEEK SPACER
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510(K) Number: K120486
Device Name: AVS AS PEEK SPACER
Manufacturer: STRYKER SPINE
Device Classification Name: intervertebral fusion device with bone graft, cervical
Regulation Number: 888.3080
Classification Product Code: ODP
Date Received: 02/17/2012
Decision Date: 08/20/2012
Regulation Medical Specialty: Orthopedic
Device Name: AVS AS PEEK SPACER
Manufacturer: STRYKER SPINE
Device Classification Name: intervertebral fusion device with bone graft, cervical
Regulation Number: 888.3080
Classification Product Code: ODP
Date Received: 02/17/2012
Decision Date: 08/20/2012
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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