FDA 510(k) Applications Submitted by K&J Consulting Corporation
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K212038 | 06/30/2021 | K&J IVA (ACIF, DLIF, PLIF, TLIF, ALIF) PEEK Cage | K&J Consulting Corporation |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact