The following data is part of a premarket notification filed by Pega Medical Inc. with the FDA for The Locking Pediatric Osteotomy Plate (lollipop) System.
| Device ID | K170704 |
| 510k Number | K170704 |
| Device Name: | The Locking Pediatric Osteotomy Plate (LolliPOP) System |
| Classification | Appliance, Fixation, Nail/blade/plate Combination, Multiple Component |
| Applicant | Pega Medical Inc. 1111 Autoroute Chomedey Iaval, CA H7w 5j8 |
| Contact | Ariel R. Dujovne |
| Correspondent | Ariel R. Dujovne Pega Medical Inc. 1111 Highway Chomedey Laval, CA H7w 5j8 |
| Product Code | KTT |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-03-08 |
| Decision Date | 2017-09-08 |
| Summary: | summary |