The following data is part of a premarket notification filed by Kls-martin L.p. with the FDA for Kls Martin Individual Patient Solutions.
| Device ID | K180962 |
| 510k Number | K180962 |
| Device Name: | KLS Martin Individual Patient Solutions |
| Classification | Plate, Bone |
| Applicant | KLS-Martin L.P. 11201 Saint Johns Industrial Parkway S Jacksonville, FL 32246 |
| Contact | Jennifer Damato |
| Correspondent | Jennifer Register Secure BioMed Evaluations 7828 Hickory Flat Highway Suite 120 Woodstock, GA 30188 |
| Product Code | JEY |
| CFR Regulation Number | 872.4760 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-04-12 |
| Decision Date | 2018-08-13 |
| Summary: | summary |