The following data is part of a premarket notification filed by Wright Medical Technology, Inc. with the FDA for Biofoam Bone Wedge.
| Device ID | K152062 |
| 510k Number | K152062 |
| Device Name: | BIOFOAM Bone Wedge |
| Classification | Plate, Fixation, Bone |
| Applicant | WRIGHT MEDICAL TECHNOLOGY, INC. 1023 Cherry Road Memphis, TN 38117 |
| Contact | Val Myles |
| Correspondent | Val Myles WRIGHT MEDICAL TECHNOLOGY, INC. 1023 Cherry Road Memphis, TN 38117 |
| Product Code | HRS |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-07-24 |
| Decision Date | 2016-05-17 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00840420163226 | K152062 | 000 |
| 00840420163219 | K152062 | 000 |
| 00840420163202 | K152062 | 000 |