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

Dynamo™ Spinal Cement; Salvo® Spine System

K Number: K260286 · Decision Jun 15, 2026
Classifications
1
FEI Numbers
80
Registration Numbers
80
Same Product Code
18
Applicant Total
59
Review Days
137

Basic Information

Device Name
Dynamo™ Spinal Cement; Salvo® Spine System
K Number
K260286
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3027
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spine Wave, Inc.
Date Received
January 29, 2026
Decision Date
June 15, 2026
Product Code
PML
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
PML Bone Cement, Posterior Screw Augmentation

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