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FDA 510(k), K220951, PMT Facet Fixation System (PMT FFS)
FDA 510(k), K220951, PMT Facet Fixation System (PMT FFS)
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510(K) Number: K220951
Device Name: PMT Facet Fixation System (PMT FFS)
Manufacturer: Providence Medical Technology, Inc
Device Classification Name: System, Facet Screw Spinal Device
Regulation Number:
Classification Product Code: MRW
Date Received: 04/01/2022
Decision Date: 12/09/2022
Regulation Medical Specialty:
Device Name: PMT Facet Fixation System (PMT FFS)
Manufacturer: Providence Medical Technology, Inc
Device Classification Name: System, Facet Screw Spinal Device
Regulation Number:
Classification Product Code: MRW
Date Received: 04/01/2022
Decision Date: 12/09/2022
Regulation Medical Specialty:
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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