The following data is part of a premarket notification filed by Surgiquip, Inc. with the FDA for Snap Oscillating Saw.
| Device ID | K931769 |
| 510k Number | K931769 |
| Device Name: | SNAP OSCILLATING SAW |
| Classification | Blade, Saw, General & Plastic Surgery, Surgical |
| Applicant | SURGIQUIP, INC. 3106 LAFAYETTE AVE. Austin, TX 78722 |
| Contact | Mary Biggers |
| Correspondent | Mary Biggers SURGIQUIP, INC. 3106 LAFAYETTE AVE. Austin, TX 78722 |
| Product Code | GFA |
| CFR Regulation Number | 878.4820 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-04-09 |
| Decision Date | 1994-01-27 |