| Primary Device ID | 20845854026875 |
| NIH Device Record Key | c444ade8-656d-415a-be25-11b9ef386480 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PINN-ACL |
| Version Model Number | CPS-8909 |
| Catalog Number | CPS-8909 |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | true |
| Expiration Date | false |
| 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(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM |
| 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 Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10845854026878 [Primary] |
| GS1 | 20845854026875 [Direct Marking] |
| LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-10-02 |
| Device Publish Date | 2020-09-24 |
| 20845854014179 | 9MM PINN-ACL CROSSPIN SYSTEM, GRAFT HARNESS WITH CANNULA |
| 20845854013806 | PINN-ACL CROSSPIN SYSTEM, 45MM (20MM) CROSSPIN |
| 20845854013653 | PINN-ACL CROSSPIN SYSTEM, 50MM (25MM) CROSSPIN |
| 20845854013646 | 8MM PINN-ACL CROSS PIN SYSTEM, GRAFT HARNESS WITH CANNULA |
| 20845854013639 | PINN-ACL CROSSPIN SYSTEM, 40MM (15MM) CROSSPIN |
| 20845854034689 | 8MM PINN-ACL CROSSPIN POSITIONING ROD |
| 20845854034672 | PINN-ACL CROSSPIN DRIVER |
| 20845854034665 | PINN-ACL CROSSPIN U-GUIDE |
| 20845854026875 | 9MM PINN-ACL CROSSPIN POSITIONING ROD |
| 20845854026868 | PINN-ACL CROSSPIN DRILL BIT |
| 20845854026851 | PINN-ACL CROSSPIN STERILIZATION TRAY |
| 20845854025519 | PINN-ACL CRUCIATE GUIDE |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PINN-ACL 74293602 1840425 Live/Registered |
CONMED CORPORATION 1992-07-13 |