Primary Device ID | 07613327627633 |
NIH Device Record Key | 8a14330e-8a88-4022-9145-c9902c81287e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | KNOTILUS+ |
Version Model Number | 3911924511 |
Catalog Number | 3911-924-511 |
Company DUNS | 187502109 |
Company Name | STRYKER CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613327627633 [Primary] |
MBI | Fastener, fixation, nondegradable, soft tissue |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-01-12 |
Device Publish Date | 2024-01-04 |
07613327623826 | PENCIL TIP OBTURATOR |
07613327623819 | OFFSET TIP GUIDE |
07613327623758 | FISHMOUTH TIP GUIDE |
07613327623734 | FORK TIP GUIDE, HIP |
07613327623727 | CROWN TIP GUIDE |
07613327623710 | BULLET TIP OBTURATOR, CANNULATED |
07613327623680 | PENCIL TIP OBTURATOR, HIP |
07613327623666 | CROWN TIP GUIDE, HIP |
07613327623659 | BULLET TIP OBTURATOR, CANNULATED, HIP |
07613327627657 | 2.9X12.5MM KNOTILUS+ ANCHOR - PEEK |
07613327627640 | 2.9X15.5MM KNOTILUS+ ANCHOR - PEEK |
07613327627633 | 2.4X11.3MM KNOTILUS+ ANCHOR - PEEK |
07613327623833 | 2.4X8.9MM DRILL, HARD BONE, HIP |
07613327623796 | 2.4X8.9MM DRILL, HIP |
07613327627701 | 2.4X8.9MM KNOTILUS+ HIP ANCHOR - PEEK |
07613327627664 | 2.9X12.5MM KNOTILUS+ HIP ANCHOR - PEEK |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
KNOTILUS+ 97615604 not registered Live/Pending |
Stryker Corporation 2022-09-30 |