The following data is part of a premarket notification filed by Medical Specialists In Packaging with the FDA for Surgical Drill Bits.
| Device ID | K831712 |
| 510k Number | K831712 |
| Device Name: | SURGICAL DRILL BITS |
| Classification | Bit, Drill |
| Applicant | MEDICAL SPECIALISTS IN PACKAGING 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HTW |
| CFR Regulation Number | 888.4540 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-05-27 |
| Decision Date | 1983-07-07 |