FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Tranquil-C Interbody System

K Number: K240416 · Decision Mar 12, 2024
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
17
Review Days
29

Basic Information

Device Name
Tranquil-C Interbody System
K Number
K240416
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nexus Spine, LLC
Date Received
February 12, 2024
Decision Date
March 12, 2024
Product Code
ODP
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
ODP Intervertebral Fusion Device With Bone Graft, Cervical

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Other Clearances by Nexus Spine, LLC

K Number Device Name
K243934 Stable-L Lumbar Interbody System
K241467 Stable-C Interbody System
K233375 Tranquil-L Interbody System
K233234 PressON Spinal Fixation System
K231486 Stable-L Standalone Lumbar Interbody System
K232530 Stable-L Standalone Lumbar Interbody System, Stable-C Interbody System
K231763 Stable-C Interbody System
K223529 PressON Spinal Fixation System
K223627 PreView-III™ Anterior Cervical Plate System
K212498 Stable-L Standalone Lumbar Interbody System
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