SSA

GUDID 00818614022444

12mm Distraction Screw

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 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 ID00818614022444
NIH Device Record Keyf51a9122-f89b-4a87-8abe-ef7c169834c5
Commercial Distribution StatusIn Commercial Distribution
Brand NameSSA
Version Model NumberDS-1210
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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Outer Diameter12 Millimeter
Outer Diameter12 Millimeter
Outer Diameter12 Millimeter
Outer Diameter12 Millimeter
Outer Diameter12 Millimeter
Outer Diameter12 Millimeter
Outer Diameter12 Millimeter
Outer Diameter12 Millimeter
Outer Diameter12 Millimeter
Outer Diameter12 Millimeter
Outer Diameter12 Millimeter
Outer Diameter12 Millimeter
Outer Diameter12 Millimeter
Outer Diameter12 Millimeter
Outer Diameter12 Millimeter
Outer Diameter12 Millimeter
Outer Diameter12 Millimeter
Outer Diameter12 Millimeter
Outer Diameter12 Millimeter
Outer Diameter12 Millimeter
Outer Diameter12 Millimeter
Outer Diameter12 Millimeter
Outer Diameter12 Millimeter
Outer Diameter12 Millimeter
Outer Diameter12 Millimeter
Outer Diameter12 Millimeter
Outer Diameter12 Millimeter
Outer Diameter12 Millimeter
Outer Diameter12 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100818614022444 [Primary]
GS110818614022441 [Package]
Package: box [10 Units]
In Commercial Distribution

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-07-12
Device Publish Date2021-07-02

On-Brand Devices [SSA]

0081861402246816mm Distraction Screw
0081861402245114mm Distraction Screw
0081861402244412mm Distraction Screw

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