Salvo™ Spine System

GUDID 10840642142150

Yoke Inserter, 4.75 mm

Spine Wave, Inc.

Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile
Primary Device ID10840642142150
NIH Device Record Keyeb3d7e40-de6c-455d-83ea-dea381533edb
Commercial Distribution StatusIn Commercial Distribution
Brand NameSalvo™ Spine System
Version Model Number10-8282
Company DUNS067789763
Company NameSpine Wave, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com
Phone203-944-9494
EmailGUDID@spinewave.com

Device Dimensions

Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter
Length30 Millimeter
Outer Diameter7.5 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS110840642142150 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NKBThoracolumbosacral Pedicle Screw System

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

[10840642142150]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-12-31
Device Publish Date2020-12-23

Devices Manufactured by Spine Wave, Inc.

10840642170887 - Exceed™ Biplanar Expandable Interbody System2023-12-19 22 mm (L) x 10 mm (W) x 9 mm (H), Lordotic 0°
10840642170894 - Exceed™ Biplanar Expandable Interbody System2023-12-19 22 mm (L) x 10 mm (W) x 10 mm (H), Lordotic 0°
10840642170900 - Exceed™ Biplanar Expandable Interbody System2023-12-19 22 mm (L) x 10 mm (W) x 11 mm (H), Lordotic 0°
10840642170917 - Exceed™ Biplanar Expandable Interbody System2023-12-19 22 mm (L) x 10 mm (W) x 12 mm (H), Lordotic 0°
10840642170924 - Exceed™ Biplanar Expandable Interbody System2023-12-19 22 mm (L) x 10 mm (W) x 13 mm (H), Lordotic 0°
10840642170931 - Exceed™ Biplanar Expandable Interbody System2023-12-19 22 mm (L) x 10 mm (W) x 14 mm (H), Lordotic 0°
10840642170948 - Exceed™ Biplanar Expandable Interbody System2023-12-19 25 mm (L) x 10 mm (W) x 9 mm (H), Lordotic 0°
10840642170955 - Exceed™ Biplanar Expandable Interbody System2023-12-19 25 mm (L) x 10 mm (W) x 10 mm (H), Lordotic 0°

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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