Osteocel

GUDID 00887517521804

Retractable Slide Tip Ins Set

Nuvasive, Inc.

Sterilization/disinfection container Sterilization/disinfection container Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable
Primary Device ID00887517521804
NIH Device Record Key993c13de-f160-4da6-b85d-e10d5f013c40
Commercial Distribution StatusIn Commercial Distribution
Brand NameOsteocel
Version Model NumberRSTINS
Company DUNS053950783
Company NameNuvasive, Inc.
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 Usefalse
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

Customer Support Contacts

Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100887517521804 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KCTSterilization wrap containers, trays, cassettes & other accessories

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00887517521804]

Moist Heat or Steam Sterilization


[00887517521804]

Moist Heat or Steam Sterilization


[00887517521804]

Moist Heat or Steam Sterilization


[00887517521804]

Moist Heat or Steam Sterilization


[00887517521804]

Moist Heat or Steam Sterilization


[00887517521804]

Moist Heat or Steam Sterilization


[00887517521804]

Moist Heat or Steam Sterilization


[00887517521804]

Moist Heat or Steam Sterilization


[00887517521804]

Moist Heat or Steam Sterilization


[00887517521804]

Moist Heat or Steam Sterilization


[00887517521804]

Moist Heat or Steam Sterilization


[00887517521804]

Moist Heat or Steam Sterilization


[00887517521804]

Moist Heat or Steam Sterilization


[00887517521804]

Moist Heat or Steam Sterilization


[00887517521804]

Moist Heat or Steam Sterilization


[00887517521804]

Moist Heat or Steam Sterilization


[00887517521804]

Moist Heat or Steam Sterilization


[00887517521804]

Moist Heat or Steam Sterilization


[00887517521804]

Moist Heat or Steam Sterilization


[00887517521804]

Moist Heat or Steam Sterilization


[00887517521804]

Moist Heat or Steam Sterilization


[00887517521804]

Moist Heat or Steam Sterilization


[00887517521804]

Moist Heat or Steam Sterilization


[00887517521804]

Moist Heat or Steam Sterilization


[00887517521804]

Moist Heat or Steam Sterilization


[00887517521804]

Moist Heat or Steam Sterilization


[00887517521804]

Moist Heat or Steam Sterilization


[00887517521804]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-09-10
Device Publish Date2016-09-23

Devices Manufactured by Nuvasive, Inc.

00887517063045 - VuePoint2024-04-15 VuePoint II Cutter, Rod
00887517063052 - SpheRx2024-04-15 SpheRx PPS Counter Torque, Reduction
00887517065216 - Precept2024-04-15 PRECEPT Handle, Fascial Splitting
00887517075376 - NVJJB2024-04-15 NVJJB EMG Harness Extensions
00887517078568 - PCM2024-04-15 PCM Slap Hammer
00887517084187 - VuePoint2024-04-15 VuePoint II Handle, Universal
00887517084644 - VuePoint2024-04-15 VP II Handle, Torque Final Tightening
00887517084675 - VuePoint2024-04-15 VP II Handle, Torque Rod-Rod Driver

Trademark Results [Osteocel]

Mark Image

Registration | Serial
Company
Trademark
Application Date
OSTEOCEL
OSTEOCEL
75521233 2470069 Live/Registered
NUVASIVE, INC.
1998-07-17

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