Primary Device ID | M739164017032 |
NIH Device Record Key | 65cdb76a-8cdb-481c-a2b4-9b6340b95677 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tower Screw Caddy Assembly |
Version Model Number | 16401-7032 |
Company DUNS | 836975784 |
Company Name | CAPTIVA SPINE, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | 561-277-9480 |
info@captivaspine.com | |
Phone | 561-277-9480 |
info@captivaspine.com | |
Phone | 561-277-9480 |
info@captivaspine.com | |
Phone | 561-277-9480 |
info@captivaspine.com | |
Phone | 561-277-9480 |
info@captivaspine.com | |
Phone | 561-277-9480 |
info@captivaspine.com | |
Phone | 561-277-9480 |
info@captivaspine.com | |
Phone | 561-277-9480 |
info@captivaspine.com | |
Phone | 561-277-9480 |
info@captivaspine.com | |
Phone | 561-277-9480 |
info@captivaspine.com | |
Phone | 561-277-9480 |
info@captivaspine.com | |
Phone | 561-277-9480 |
info@captivaspine.com | |
Phone | 561-277-9480 |
info@captivaspine.com | |
Phone | 561-277-9480 |
info@captivaspine.com | |
Phone | 561-277-9480 |
info@captivaspine.com | |
Phone | 561-277-9480 |
info@captivaspine.com | |
Phone | 561-277-9480 |
info@captivaspine.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | M739164017032 [Primary] |
FSM | Tray, Surgical, Instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[M739164017032]
Moist Heat or Steam Sterilization
[M739164017032]
Moist Heat or Steam Sterilization
[M739164017032]
Moist Heat or Steam Sterilization
[M739164017032]
Moist Heat or Steam Sterilization
[M739164017032]
Moist Heat or Steam Sterilization
[M739164017032]
Moist Heat or Steam Sterilization
[M739164017032]
Moist Heat or Steam Sterilization
[M739164017032]
Moist Heat or Steam Sterilization
[M739164017032]
Moist Heat or Steam Sterilization
[M739164017032]
Moist Heat or Steam Sterilization
[M739164017032]
Moist Heat or Steam Sterilization
[M739164017032]
Moist Heat or Steam Sterilization
[M739164017032]
Moist Heat or Steam Sterilization
[M739164017032]
Moist Heat or Steam Sterilization
[M739164017032]
Moist Heat or Steam Sterilization
[M739164017032]
Moist Heat or Steam Sterilization
[M739164017032]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-10-09 |
Device Publish Date | 2023-09-29 |
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M739985221229 - TransFasten | 2024-03-19 LD (.125” Wire) Marking Pin, 229mm, Non-Threaded Trocar |
M739985221305 - TransFasten | 2024-03-19 LD (.125” Wire) Marking Pin, 305mm, Non-Threaded Trocar |
M739985222229 - TransFasten | 2024-03-19 LD (.125” Wire) Marking Pin, 229mm, Conical Blunt |
M73910110250 - TransFasten - LSF (Lateral Sacroiliac Fusion System) | 2024-03-11 Sacroiliac Immobilization Device - 9mm (D) x 25mm (L) |
M73910110300 - TransFasten - LSF (Lateral Sacroiliac Fusion System) | 2024-03-11 Sacroiliac Immobilization Device - 9mm (D) x 30mm (L) |
M73910110350 - TransFasten - LSF (Lateral Sacroiliac Fusion System) | 2024-03-11 Sacroiliac Immobilization Device - 9mm (D) x 35mm (L) |
M73910110400 - TransFasten - LSF (Lateral Sacroiliac Fusion System) | 2024-03-11 Sacroiliac Immobilization Device - 9mm (D) x 40mm (L) |