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

Tranquil-L Interbody System

K Number: K233375 · Decision Mar 20, 2024
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
17
Review Days
170

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Basic Information

Device Name
Tranquil-L Interbody System
K Number
K233375
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
October 2, 2023
Decision Date
March 20, 2024
Product Code
MAX
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MAX), ordered by most recent decision date.

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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
K240416 Tranquil-C 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
Search all 17 clearances from Nexus Spine, LLC →