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

Genesys Spine 3DP Lumbar Interbody System

K Number: K182987 · Decision Dec 12, 2019
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
31
Review Days
409

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Basic Information

Device Name
Genesys Spine 3DP Lumbar Interbody System
K Number
K182987
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Genesys Spine
Date Received
October 29, 2018
Decision Date
December 12, 2019
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

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Other Clearances by Genesys Spine

K Number Device Name
K252322 SIros-X System
K242483 Genesys Spine AIS-C II Cervical Interbody Fusion System
K233595 Genesys Spine Sacroiliac Joint Fusion System with Navigation
K233594 Genesys Spine 3DP AIS-C II Cervical Interbody System
K220096 Genesys Spine 3DP Lumbar Interbody System
K191489 Genesys Spine 3DP Cervical Interbody System
K192678 Genesys Spine Binary® Lumbar Plate System
K191748 Genesys Spine Sacroiliac Joint Fusion System
K192076 Binary® Anterior Cervical Plate System
K181295 Genesys Spine AIS-C Cervical Stand-Alone System
Search all 31 clearances from Genesys Spine →