The following data is part of a premarket notification filed by Landos, Inc. with the FDA for Twist-off Screw.
| Device ID | K962233 |
| 510k Number | K962233 |
| Device Name: | TWIST-OFF SCREW |
| Classification | Screw, Fixation, Bone |
| Applicant | LANDOS, INC. 9109 COPENHAVER DR. Potomac, MD 20854 |
| Contact | Norman F Estrin |
| Correspondent | Norman F Estrin LANDOS, INC. 9109 COPENHAVER DR. Potomac, MD 20854 |
| Product Code | HWC |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-06-11 |
| Decision Date | 1996-10-03 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00887868011238 | K962233 | 000 |
| 00887868011221 | K962233 | 000 |
| 00887868011214 | K962233 | 000 |
| 00887868011207 | K962233 | 000 |
| 00887868011191 | K962233 | 000 |
| 00887868116179 | K962233 | 000 |
| 00887868116162 | K962233 | 000 |
| 00887868116155 | K962233 | 000 |
| 00887868116148 | K962233 | 000 |