Osteolock 5260-5-028

GUDID 07613327035704

3.5mm Hex Drive Head Cancellous Screw

Howmedica Osteonics Corp.

Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding)
Primary Device ID07613327035704
NIH Device Record Keya72a587b-8818-4950-84ff-6af3d88e971b
Commercial Distribution StatusIn Commercial Distribution
Brand NameOsteolock
Version Model Number5260-5-028
Catalog Number5260-5-028
Company DUNS058311945
Company NameHowmedica Osteonics Corp.
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

Device Dimensions

Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter
Device Size Text, specify0
Length28 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS107613327035704 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JDIProsthesis, hip, semi-constrained, metal/polymer, cemented

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-09-24

On-Brand Devices [Osteolock]

076133270357593.5mm Hex Drive Head Cancellous Screw
076133270357423.5mm Hex Drive Head Cancellous Screw
076133270357353.5mm Hex Drive Head Cancellous Screw
076133270357283.5mm Hex Drive Head Cancellous Screw
076133270357113.5mm Hex Drive Head Cancellous Screw
076133270357043.5mm Hex Drive Head Cancellous Screw
076133270356983.5mm Hex Drive Head Cancellous Screw
076133270356813.5mm Hex Drive Head Cancellous Screw
076133270356743.5mm Hex Drive Head Cancellous Screw
076133270356673.5mm Hex Drive Head Cancellous Screw
076133270356503.5mm Hex Drive Head Cancellous Screw
076133270356433.5mm Hex Drive Head Cancellous Screw
076133270356363.5mm Hex Drive Head Cancellous Screw
076133270356293.5mm Hex Drive Head Cancellous Screw

Trademark Results [Osteolock]

Mark Image

Registration | Serial
Company
Trademark
Application Date
OSTEOLOCK
OSTEOLOCK
77518307 3793867 Dead/Cancelled
Bacterin International, Inc
2008-07-09

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