Primary Device ID | M73924714975 |
NIH Device Record Key | 42b4a2e1-9c94-435d-b53a-2e8fc5f926ae |
Commercial Distribution Discontinuation | 2017-08-08 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Cross Connector, Large |
Version Model Number | 2471-4975 |
Company DUNS | 836975784 |
Company Name | CAPTIVA SPINE, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | M73924714975 [Primary] |
MNH | Orthosis, Spondylolisthesis Spinal Fixation |
Steralize Prior To Use | true |
Device Is Sterile | false |
[M73924714975]
Moist Heat or Steam Sterilization
[M73924714975]
Moist Heat or Steam Sterilization
[M73924714975]
Moist Heat or Steam Sterilization
[M73924714975]
Moist Heat or Steam Sterilization
[M73924714975]
Moist Heat or Steam Sterilization
[M73924714975]
Moist Heat or Steam Sterilization
[M73924714975]
Moist Heat or Steam Sterilization
[M73924714975]
Moist Heat or Steam Sterilization
[M73924714975]
Moist Heat or Steam Sterilization
[M73924714975]
Moist Heat or Steam Sterilization
[M73924714975]
Moist Heat or Steam Sterilization
[M73924714975]
Moist Heat or Steam Sterilization
[M73924714975]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2023-09-18 |
Device Publish Date | 2015-10-30 |
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