SPINAL TOUCH
Goniometer, Ac-powered
FASSTECH
The following data is part of a premarket notification filed by Fasstech with the FDA for Spinal Touch.
Pre-market Notification Details
| Device ID | K961212 |
| 510k Number | K961212 |
| Device Name: | SPINAL TOUCH |
| Classification | Goniometer, Ac-powered |
| Applicant | FASSTECH 155 MIDDLESEX TURNPIKE Burlington, MA 01803 |
| Contact | Lee R Brody |
| Correspondent | Lee R Brody FASSTECH 155 MIDDLESEX TURNPIKE Burlington, MA 01803 |
| Product Code | KQX |
| CFR Regulation Number | 888.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-03-28 |
| Decision Date | 1996-06-12 |
Trademark Results [SPINAL TOUCH]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SPINAL TOUCH 76193911 2563459 Dead/Cancelled |
Hudson, Tom 2001-01-11 |
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