The following data is part of a premarket notification filed by Conmed Corporation with the FDA for Trushot With Y-knot All-suture Anchor.
Device ID | K182446 |
510k Number | K182446 |
Device Name: | TruShot With Y-Knot All-Suture Anchor |
Classification | Fastener, Fixation, Nondegradable, Soft Tissue |
Applicant | ConMed Corporation 525 French Road Utica, NY 13502 |
Contact | Diana L. Nader-martone |
Correspondent | Diana L. Nader-martone ConMed Corporation 525 French Road Utica, NY 13502 |
Product Code | MBI |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-09-07 |
Decision Date | 2018-12-19 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
30845854850071 | K182446 | 000 |
30845854850064 | K182446 | 000 |
20845854648985 | K182446 | 000 |
20845854648503 | K182446 | 000 |
20653405988394 | K182446 | 000 |
20653405988387 | K182446 | 000 |