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 |