FDA 510(k), K121741, 4-WEB CERVICAL STS (SPINAL TRUSS SYSTEM)

FDA 510(k), K121741, 4-WEB CERVICAL STS (SPINAL TRUSS SYSTEM)

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510(K) Number: K121741
Device Name: 4-WEB CERVICAL STS (SPINAL TRUSS SYSTEM)
Manufacturer: 4-WEB, INC.
Device Classification Name: intervertebral fusion device with bone graft, cervical
Regulation Number: 888.3080
Classification Product Code: ODP
Date Received: 06/13/2012
Decision Date: 10/18/2012
Regulation Medical Specialty: Orthopedic
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