Primary Device ID | 07613327169379 |
NIH Device Record Key | ae25d5d6-de16-409a-8f67-9e4ab88c4010 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | DBK9CC |
Catalog Number | DBK9CC |
Company DUNS | 078470558 |
Company Name | STRYKER CORPORATION |
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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613327169379 [Primary] |
DWJ | System, thermal regulating |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-03-21 |
Device Publish Date | 2016-09-24 |
07613327661989 - KNOTILUS+ | 2025-06-24 2.9X15.5MM KNOTILUS+ ANCHOR - BIOCOMPOSITE |
07613327661996 - KNOTILUS+ | 2025-06-24 2.4X8.9MM KNOTILUS+ HIP ANCHOR - BIOCOMPOSITE |
07613327662009 - KNOTILUS+ | 2025-06-24 2.4X11.3MM KNOTILUS+ ANCHOR - BIOCOMPOSITE |
07613327662016 - KNOTILUS+ | 2025-06-24 2.9X12.5MM KNOTILUS+ HIP ANCHOR - BIOCOMPOSITE |
07613327662023 - KNOTILUS+ | 2025-06-24 2.9X12.5MM KNOTILUS+ ANCHOR - BIOCOMPOSITE |
07613327662030 - ALPHAVENT | 2025-06-24 ALPHAVENT KNOTLESS SP, 4.75MM, BIOCOMPOSITE ANCHOR |
07613327662047 - ALPHAVENT | 2025-06-24 ALPHAVENT KNOTLESS SP, 5.5MM, BIOCOMPOSITE ANCHOR |
07613327662054 - ALPHAVENT | 2025-06-24 ALPHAVENT KNOTLESS SP, 6.5MM, BIOCOMPOSITE ANCHOR |