The following data is part of a premarket notification filed by Pin Dot Products, Inc. with the FDA for Impala Axles.
| Device ID | K913511 | 
| 510k Number | K913511 | 
| Device Name: | IMPALA AXLES | 
| Classification | Components, Wheelchair | 
| Applicant | PIN DOT PRODUCTS, INC. 6001 GROSS POINT RD. Niles, IL 60648 -4027 | 
| Product Code | KNN | 
| CFR Regulation Number | 890.3920 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 1991-08-07 | 
| Decision Date | 1991-09-05 |