SeaSpine Spacer System - Pacifica 93-3617

GUDID 10889981089368

Long Bullet Distractor, 9mm

SEASPINE ORTHOPEDICS CORPORATION

Orthopaedic surgical distractor, internal
Primary Device ID10889981089368
NIH Device Record Key06a79903-d64c-4d68-8684-fc6263eb995a
Commercial Distribution StatusIn Commercial Distribution
Brand NameSeaSpine Spacer System - Pacifica
Version Model Number93-3617
Catalog Number93-3617
Company DUNS079840876
Company NameSEASPINE ORTHOPEDICS 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 Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS110889981089368 [Primary]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10889981089368]

Moist Heat or Steam Sterilization

[10889981089368]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-03-31

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