Type A Broach Size 15

GUDID 09348215055752

SIGNATURE ORTHOPAEDICS PTY LTD

Orthopaedic broach
Primary Device ID09348215055752
NIH Device Record Key24b08c6d-50dd-4694-b65c-3a2bf3bbb368
Commercial Distribution StatusIn Commercial Distribution
Brand NameType A Broach Size 15
Version Model Number111-18-1508
Company DUNS751993028
Company NameSIGNATURE ORTHOPAEDICS PTY LTD
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

Device Identifiers

Device Issuing AgencyDevice ID
GS109348215055752 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[09348215055752]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-11-07
Device Publish Date2019-10-30

Devices Manufactured by SIGNATURE ORTHOPAEDICS PTY LTD

09348215129224 - Verteloc Lumbar Cage 2024-03-20
09348215129231 - Verteloc Lumbar Cage 2024-03-20
09348215129248 - Verteloc Lumbar Cage 2024-03-20
09348215129255 - Verteloc Lumbar Cage 2024-03-20
09348215129262 - Verteloc Lumbar Cage 2024-03-20
09348215129279 - Verteloc Lumbar Cage 2024-03-20
09348215129286 - Verteloc Lumbar Cage 2024-03-20
09348215129293 - Verteloc Lumbar Cage 2024-03-20

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