The following data is part of a premarket notification filed by Ethicon Endo-surgery, Inc. with the FDA for Endopath Non-bladed Obturator Trocar System (5 Mm).
Device ID | K011257 |
510k Number | K011257 |
Device Name: | ENDOPATH NON-BLADED OBTURATOR TROCAR SYSTEM (5 MM) |
Classification | Laparoscope, General & Plastic Surgery |
Applicant | ETHICON ENDO-SURGERY, INC. 4545 CREEK RD. Cincinnati, OH 45242 -2839 |
Contact | Katie Fordyce |
Correspondent | Katie Fordyce ETHICON ENDO-SURGERY, INC. 4545 CREEK RD. Cincinnati, OH 45242 -2839 |
Product Code | GCJ |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-04-24 |
Decision Date | 2001-07-13 |