Distraction Screw, 14MM pouch

GUDID 00818614022567

Synergy Distraction Screw, 14MM pouch

Maruho Medical, Inc.

Intraoperative bone pin/screw, sterile Intraoperative bone pin/screw, sterile Intraoperative bone pin/screw, sterile Intraoperative bone pin/screw, sterile Intraoperative bone pin/screw, sterile Intraoperative bone pin/screw, sterile Intraoperative bone pin/screw, sterile Intraoperative bone pin/screw, sterile Intraoperative bone pin/screw, sterile Intraoperative bone pin/screw, sterile Intraoperative bone pin/screw, sterile Intraoperative bone pin/screw, sterile Intraoperative bone pin/screw, sterile Intraoperative bone pin/screw, sterile Intraoperative bone pin/screw, sterile Intraoperative bone pin/screw, sterile Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use
Primary Device ID00818614022567
NIH Device Record Keyf085a90b-16f2-4ecd-aae5-7753058d04c6
Commercial Distribution StatusIn Commercial Distribution
Brand NameDistraction Screw, 14MM pouch
Version Model NumberSM-14
Company DUNS117630237
Company NameMaruho Medical, Inc.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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 Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100818614022567 [Primary]
GS110818614022564 [Package]
Package: Box [5 Units]
In Commercial Distribution

FDA Product Code

LYQAccessories, Fixation, Spinal Intervertebral Body

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-09-09
Device Publish Date2022-09-01

On-Brand Devices [Distraction Screw, 14MM pouch]

10818614022588Surgix Distraction Screw, 14MM pouch
00818614022567Synergy Distraction Screw, 14MM pouch

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.