The following data is part of a premarket notification filed by Li Medical Technologies, Inc. with the FDA for Lmt Bone Anchor.
| Device ID | K951233 |
| 510k Number | K951233 |
| Device Name: | LMT BONE ANCHOR |
| Classification | Screw, Fixation, Bone |
| Applicant | LI MEDICAL TECHNOLOGIES, INC. 4 ARMSTRONG RD. Shelton, CT 06484 |
| Contact | Rhodemann Li |
| Correspondent | Rhodemann Li LI MEDICAL TECHNOLOGIES, INC. 4 ARMSTRONG RD. Shelton, CT 06484 |
| Product Code | HWC |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-03-20 |
| Decision Date | 1995-07-03 |