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FDA 510(k), K203503, Camber Sacroiliac (SI) Fixation System
FDA 510(k), K203503, Camber Sacroiliac (SI) Fixation System
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510(K) Number: K203503
Device Name: Camber Sacroiliac (SI) Fixation System
Manufacturer: Camber Spine Technologies, LLC
Device Classification Name: Sacroiliac Joint Fixation
Regulation Number: 888.3040
Classification Product Code: OUR
Date Received: 11/30/2020
Decision Date: 09/02/2022
Regulation Medical Specialty: Orthopedic
Device Name: Camber Sacroiliac (SI) Fixation System
Manufacturer: Camber Spine Technologies, LLC
Device Classification Name: Sacroiliac Joint Fixation
Regulation Number: 888.3040
Classification Product Code: OUR
Date Received: 11/30/2020
Decision Date: 09/02/2022
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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