The following data is part of a premarket notification filed by Sutter Corp. with the FDA for Model 9000 At Ankle Cpm Device.
| Device ID | K902707 |
| 510k Number | K902707 |
| Device Name: | MODEL 9000 AT ANKLE CPM DEVICE |
| Classification | Exerciser, Powered |
| Applicant | SUTTER CORP. 9425 CHESAPEAKE DR. San Diego, CA 92123 |
| Contact | William Townsend |
| Correspondent | William Townsend SUTTER CORP. 9425 CHESAPEAKE DR. San Diego, CA 92123 |
| Product Code | BXB |
| CFR Regulation Number | 890.5380 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-06-19 |
| Decision Date | 1990-07-25 |