Salvo™ Spine System

Thoracolumbosacral Pedicle Screw System

Spine Wave, Inc.

The following data is part of a premarket notification filed by Spine Wave, Inc. with the FDA for Salvo™ Spine System.

Pre-market Notification Details

Device IDK182954
510k NumberK182954
Device Name:Salvo™ Spine System
ClassificationThoracolumbosacral Pedicle Screw System
Applicant Spine Wave, Inc. 3 Enterprise Drive, Suite 210 Shelton,  CT  06484
ContactAmy Noccioli
CorrespondentAmy Noccioli
Spine Wave, Inc. 3 Enterprise Drive, Suite 210 Shelton,  CT  06484
Product CodeNKB  
CFR Regulation Number888.3070 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2018-10-24
Decision Date2018-12-12
Summary:summary

NIH GUDID Devices

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Trademark Results [Salvo]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SALVO
SALVO
90904543 not registered Live/Pending
S.S. Steiner, Inc.
2021-08-26
SALVO
SALVO
90320539 not registered Live/Pending
Flatrock Brands LLC
2020-11-16
SALVO
SALVO
88781895 not registered Live/Pending
lauren king salvo
2020-02-01
SALVO
SALVO
88347085 not registered Live/Pending
High Threat Concealment, LLC
2019-03-19
SALVO
SALVO
88072149 not registered Live/Pending
Digital Iris LLC
2018-08-09
SALVO
SALVO
87597515 not registered Live/Pending
Spine Wave, Inc.
2017-09-06
SALVO
SALVO
87433965 not registered Live/Pending
26 California Wholesale, Inc.
2017-05-02
SALVO
SALVO
86816832 5142914 Live/Registered
Gensco Laboratories, LLC
2015-11-11
SALVO
SALVO
86801075 5056101 Live/Registered
Michigan Tube Swagers and Fabricators, Inc.
2015-10-27
SALVO
SALVO
86566258 5214499 Live/Registered
Promika, LLC
2015-03-17
SALVO
SALVO
86389467 5658674 Live/Registered
Silencerco LLC
2014-09-09
SALVO
SALVO
86376775 not registered Dead/Abandoned
Torbay Brands LLC
2014-08-26

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