The following data is part of a premarket notification filed by Concept, Inc. with the FDA for Interference Screw.
| Device ID | K874676 |
| 510k Number | K874676 |
| Device Name: | INTERFERENCE SCREW |
| Classification | Screw, Fixation, Bone |
| Applicant | CONCEPT, INC. 12707 U.S. 19 SOUTH Clearwater, FL 33546 |
| Contact | Lori Colvin |
| Correspondent | Lori Colvin CONCEPT, INC. 12707 U.S. 19 SOUTH Clearwater, FL 33546 |
| Product Code | HWC |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-11-13 |
| Decision Date | 1988-03-07 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20845854015220 | K874676 | 000 |
| 20845854014094 | K874676 | 000 |
| 20845854014032 | K874676 | 000 |
| 20845854014025 | K874676 | 000 |
| 20845854013882 | K874676 | 000 |
| 20845854013783 | K874676 | 000 |
| 20845854013769 | K874676 | 000 |
| 20845854013691 | K874676 | 000 |
| 20845854013585 | K874676 | 000 |
| 20845854012502 | K874676 | 000 |
| 10845854014837 | K874676 | 000 |
| 20845854014148 | K874676 | 000 |
| 20845854014155 | K874676 | 000 |
| 20845854014216 | K874676 | 000 |
| 20845854015213 | K874676 | 000 |
| 20845854015060 | K874676 | 000 |
| 20845854014780 | K874676 | 000 |
| 20845854014766 | K874676 | 000 |
| 20845854014629 | K874676 | 000 |
| 20845854014612 | K874676 | 000 |
| 20845854014483 | K874676 | 000 |
| 20845854014384 | K874676 | 000 |
| 20845854014278 | K874676 | 000 |
| 20845854014261 | K874676 | 000 |
| 30845854014831 | K874676 | 000 |