BIOCRYL 231720
GUDID 10886705010622
BIOCRYL INTERFERENCE SCREW Absorbable - TCP/PLA 9 x 23mm
DEPUY MITEK, LLC
Orthopaedic bone screw, bioabsorbable| Primary Device ID | 10886705010622 |
| NIH Device Record Key | 51e4a0c7-fdd3-4acf-96ea-4f3b74d75541 |
| Commercial Distribution Discontinuation | 2021-01-28 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BIOCRYL |
| Version Model Number | 231720 |
| Catalog Number | 231720 |
| Company DUNS | 190572854 |
| Company Name | DEPUY MITEK, LLC |
| 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 | 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(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10886705010622 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K013572
FDA Product Code
| HWC | Screw, fixation, bone |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2021-01-07 |
| Device Publish Date | 2015-09-01 |
On-Brand Devices [BIOCRYL]
| 10886705010660 | BIOCRYL INTERFERENCE SCREW Absorbable - TCP/PLA 11 x 30mm |
| 10886705010653 | BIOCRYL INTERFERENCE SCREW Absorbable - TCP/PLA 10 x 30mm |
| 10886705010646 | BIOCRYL INTERFERENCE SCREW Absorbable - TCP/PLA 10 x 23mm |
| 10886705010639 | BIOCRYL INTERFERENCE SCREW Absorbable - TCP/PLA 9 x 30mm |
| 10886705010622 | BIOCRYL INTERFERENCE SCREW Absorbable - TCP/PLA 9 x 23mm |
| 10886705010615 | BIOCRYL INTERFERENCE SCREW Absorbable - TCP/PLA 8 x 30mm |
| 10886705010608 | BIOCRYL INTERFERENCE SCREW Absorbable - TCP/PLA 8 x 23mm |
| 10886705010592 | BIOCRYL INTERFERENCE SCREW Absorbable - TCP/PLA 7 x 30mm |
| 10886705010585 | BIOCRYL INTERFERENCE SCREW Absorbable - TCP/PLA 7 x 23mm |
| 10886705006977 | STARTER TAP BIOCRYL INTERFERENCE SCREW |
Trademark Results [BIOCRYL]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 BIOCRYL 87953900 not registered Live/Pending |
Johnson & Johnson 2018-06-08 |
 BIOCRYL 86290453 5519788 Live/Registered |
Johnson & Johnson 2014-05-23 |
 BIOCRYL 76401695 2789568 Dead/Cancelled |
JOHNSON & JOHNSON 2002-04-23 |
 BIOCRYL 73663668 1480319 Dead/Cancelled |
ROHM AND HAAS COMPANY 1987-05-29 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.