Primary Device ID | 00190837016951 |
NIH Device Record Key | ebeec09c-5c5b-440a-904d-283188e697e0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Solstice Occipito-Cervico-Thoracic System |
Version Model Number | 9240-12 |
Company DUNS | 183641617 |
Company Name | Life Spine, Inc. |
Device Count | 1 |
DM Exempt | true |
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 |
---|---|
GS1 | 00190837016951 [Primary] |
KWP | Appliance, Fixation, Spinal Interlaminal |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00190837016951]
Moist Heat or Steam Sterilization
[00190837016951]
Moist Heat or Steam Sterilization
[00190837016951]
Moist Heat or Steam Sterilization
[00190837016951]
Moist Heat or Steam Sterilization
[00190837016951]
Moist Heat or Steam Sterilization
[00190837016951]
Moist Heat or Steam Sterilization
[00190837016951]
Moist Heat or Steam Sterilization
[00190837016951]
Moist Heat or Steam Sterilization
[00190837016951]
Moist Heat or Steam Sterilization
[00190837016951]
Moist Heat or Steam Sterilization
[00190837016951]
Moist Heat or Steam Sterilization
[00190837016951]
Moist Heat or Steam Sterilization
[00190837016951]
Moist Heat or Steam Sterilization
[00190837016951]
Moist Heat or Steam Sterilization
[00190837016951]
Moist Heat or Steam Sterilization
[00190837016951]
Moist Heat or Steam Sterilization
[00190837016951]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-12-20 |