0306621000

GUDID 07613252639794

Curette

STRYKER CORPORATION

Spinal curette Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use
Primary Device ID07613252639794
NIH Device Record Keya11e2265-48e7-4e75-a529-042b47f0901c
Commercial Distribution StatusIn Commercial Distribution
Version Model Number0306621000
Catalog Number0306621000
Company DUNS196548481
Company NameSTRYKER CORPORATION
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

Customer Support Contacts

Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com

Device Dimensions

Needle Gauge11 Gauge
Needle Gauge11 Gauge
Needle Gauge11 Gauge
Needle Gauge11 Gauge
Needle Gauge11 Gauge
Needle Gauge11 Gauge
Needle Gauge11 Gauge
Needle Gauge11 Gauge
Needle Gauge11 Gauge
Needle Gauge11 Gauge
Needle Gauge11 Gauge
Needle Gauge11 Gauge
Needle Gauge11 Gauge
Needle Gauge11 Gauge
Needle Gauge11 Gauge
Needle Gauge11 Gauge
Needle Gauge11 Gauge
Needle Gauge11 Gauge
Needle Gauge11 Gauge

Device Identifiers

Device Issuing AgencyDevice ID
GS107613252639794 [Primary]

FDA Product Code

OCJspinal channeling instrument, vertebroplasty

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-10-25
Device Publish Date2018-09-24

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07613327627664 - KNOTILUS+2024-03-15 2.9X12.5MM KNOTILUS+ HIP ANCHOR - PEEK
07613327627701 - KNOTILUS+2024-03-15 2.4X8.9MM KNOTILUS+ HIP ANCHOR - PEEK
07613327623796 - KNOTILUS+2024-03-13 2.4X8.9MM DRILL, HIP
07613327623833 - KNOTILUS+2024-03-13 2.4X8.9MM DRILL, HARD BONE, HIP
07613327634686 - Iconix2024-03-12 Iconix DC Guide for 1.4mm anchor
07613327634693 - Iconix2024-03-12
07613327616675 - SPY2024-03-06
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