Primary Device ID | M739FPT01000 |
NIH Device Record Key | f6e6e439-baa5-4bb1-b500-f5f57984ce38 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Inserter Base |
Version Model Number | FPT0100 |
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 | false |
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 | 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 | |
Phone | 561-277-9480 |
info@captivaspine.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | M739FPT01000 [Primary] |
LXH | Orthopedic Manual Surgical Instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[M739FPT01000]
Moist Heat or Steam Sterilization
[M739FPT01000]
Moist Heat or Steam Sterilization
[M739FPT01000]
Moist Heat or Steam Sterilization
[M739FPT01000]
Moist Heat or Steam Sterilization
[M739FPT01000]
Moist Heat or Steam Sterilization
[M739FPT01000]
Moist Heat or Steam Sterilization
[M739FPT01000]
Moist Heat or Steam Sterilization
[M739FPT01000]
Moist Heat or Steam Sterilization
[M739FPT01000]
Moist Heat or Steam Sterilization
[M739FPT01000]
Moist Heat or Steam Sterilization
[M739FPT01000]
Moist Heat or Steam Sterilization
[M739FPT01000]
Moist Heat or Steam Sterilization
[M739FPT01000]
Moist Heat or Steam Sterilization
[M739FPT01000]
Moist Heat or Steam Sterilization
[M739FPT01000]
Moist Heat or Steam Sterilization
[M739FPT01000]
Moist Heat or Steam Sterilization
[M739FPT01000]
Moist Heat or Steam Sterilization
[M739FPT01000]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-10-24 |
Device Publish Date | 2023-10-16 |
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M73910110400 - TransFasten - LSF (Lateral Sacroiliac Fusion System) | 2024-03-11 Sacroiliac Immobilization Device - 9mm (D) x 40mm (L) |