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

Lateral Spine Truss System (LSTS) Interbody Fusion Device

K Number: K211388 · Decision Aug 5, 2021
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
11
Review Days
92

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Basic Information

Device Name
Lateral Spine Truss System (LSTS) Interbody Fusion Device
K Number
K211388
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
4Web Medical, Inc.
Date Received
May 5, 2021
Decision Date
August 5, 2021
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 4Web Medical, Inc.

K Number Device Name
K253200 Cervical Spine Truss System - Stand Alone (CSTS-SA)
K240388 Osteotomy Truss System (OTS)
K233966 Anterior Spine Truss System-Stand Alone (ASTS-SA)
K230088 Ankle Truss System (ATS)
K231739 Cervical Spine Truss System (CSTS)
K223362 Cervical Spine Truss System - Stand Alone (CSTS-SA) Interbody Fusion Device
K221266 Cervical Spine Truss System (CSTS) Interbody Fusion Device
K221283 Hammertoe Truss System (HTS)
K220463 Osteotomy Truss System (OTS)
K212527 Cervical Spine Truss System Plating Solution (CSTS-PS)
Search all 11 clearances from 4Web Medical, Inc. →