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

Invictus Bands System

K Number: K253615 · Decision Mar 25, 2026
Classifications
1
FEI Numbers
65
Registration Numbers
65
Same Product Code
36
Applicant Total
93
Review Days
127

Basic Information

Device Name
Invictus Bands System
K Number
K253615
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3010
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Alphatec Spine, Inc.
Date Received
November 18, 2025
Decision Date
March 25, 2026
Product Code
OWI
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
OWI Bone Fixation Cerclage, Sublaminar

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Other Clearances by Alphatec Spine, Inc.

K Number Device Name
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K252842 SafeOp 3: Neural Informatix System
K251965 Proximity Anterior Cervical Plate System; Segmental Plating System (SPS)
K251080 IdentiTi II Cervical Interbody System
K243461 Calibrate Interbody Systems
K242364 IdentiTi™ II Interbody System
K242147 Calibrate LTX Interbody System; Calibrate NanoTec LTX Interbody System
K241519 Invictus® Small Stature Spinal Fixation System
K240199 IntraOp Alignment System
K234092 SafeOp 3: Neural Informatix Systeem
Search all 93 clearances from Alphatec Spine, Inc. →