KNOTILUS+ 3911-829-512
GUDID 07613327662023
2.9X12.5MM KNOTILUS+ ANCHOR - BIOCOMPOSITE
STRYKER CORPORATION
Tendon/ligament bone anchor, bioabsorbable| Primary Device ID | 07613327662023 |
| NIH Device Record Key | fea9f512-edd2-451e-9683-3aacfad8e811 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | KNOTILUS+ |
| Version Model Number | 3911-829-512 |
| Catalog Number | 3911-829-512 |
| 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 |
Customer Support Contacts
| 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 Dimensions
| 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 |
Operating and Storage Conditions
| Handling Environment Temperature | Between 0 and 32 Degrees Celsius |
| Storage Environment Temperature | Between 0 and 32 Degrees Celsius |
| Handling Environment Temperature | Between 0 and 32 Degrees Celsius |
| Storage Environment Temperature | Between 0 and 32 Degrees Celsius |
| Handling Environment Temperature | Between 0 and 32 Degrees Celsius |
| Storage Environment Temperature | Between 0 and 32 Degrees Celsius |
| Handling Environment Temperature | Between 0 and 32 Degrees Celsius |
| Storage Environment Temperature | Between 0 and 32 Degrees Celsius |
| Handling Environment Temperature | Between 0 and 32 Degrees Celsius |
| Storage Environment Temperature | Between 0 and 32 Degrees Celsius |
| Handling Environment Temperature | Between 0 and 32 Degrees Celsius |
| Storage Environment Temperature | Between 0 and 32 Degrees Celsius |
| Handling Environment Temperature | Between 0 and 32 Degrees Celsius |
| Storage Environment Temperature | Between 0 and 32 Degrees Celsius |
| Handling Environment Temperature | Between 0 and 32 Degrees Celsius |
| Storage Environment Temperature | Between 0 and 32 Degrees Celsius |
| Handling Environment Temperature | Between 0 and 32 Degrees Celsius |
| Storage Environment Temperature | Between 0 and 32 Degrees Celsius |
| Handling Environment Temperature | Between 0 and 32 Degrees Celsius |
| Storage Environment Temperature | Between 0 and 32 Degrees Celsius |
| Handling Environment Temperature | Between 0 and 32 Degrees Celsius |
| Storage Environment Temperature | Between 0 and 32 Degrees Celsius |
| Handling Environment Temperature | Between 0 and 32 Degrees Celsius |
| Storage Environment Temperature | Between 0 and 32 Degrees Celsius |
| Handling Environment Temperature | Between 0 and 32 Degrees Celsius |
| Storage Environment Temperature | Between 0 and 32 Degrees Celsius |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327662023 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K250544
FDA Product Code
| MAI | Fastener, fixation, biodegradable, soft tissue |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-06-24 |
| Device Publish Date | 2025-06-16 |
On-Brand Devices [KNOTILUS+]
| 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 |
| 07613327662023 | 2.9X12.5MM KNOTILUS+ ANCHOR - BIOCOMPOSITE |
| 07613327662016 | 2.9X12.5MM KNOTILUS+ HIP ANCHOR - BIOCOMPOSITE |
| 07613327662009 | 2.4X11.3MM KNOTILUS+ ANCHOR - BIOCOMPOSITE |
| 07613327661996 | 2.4X8.9MM KNOTILUS+ HIP ANCHOR - BIOCOMPOSITE |
| 07613327661989 | 2.9X15.5MM KNOTILUS+ ANCHOR - BIOCOMPOSITE |
Trademark Results [KNOTILUS+]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 KNOTILUS+ 97615604 not registered Live/Pending |
Stryker Corporation 2022-09-30 |
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