12mm Distraction Pin 301.912

GUDID 10850014548008

12mm Distraction Pin Quantity 10 DI 00850014548001

FOLSOM METAL PRODUCTS, INC.

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 ID10850014548008
NIH Device Record Key944a837a-abbb-4b0f-b624-c45b035c6b33
Commercial Distribution StatusIn Commercial Distribution
Brand Name12mm Distraction Pin
Version Model Number301.912
Catalog Number301.912
Company DUNS878146737
Company NameFOLSOM METAL PRODUCTS, 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 Identifiers

Device Issuing AgencyDevice ID
GS110850014548008 [Primary]

FDA Product Code

GCZRetainer, Surgical

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-03-26
Device Publish Date2020-03-18

On-Brand Devices [12mm Distraction Pin ]

0085001454800112mm Distraction Pin
1085001454800812mm Distraction Pin Quantity 10 DI 00850014548001

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