The following data is part of a premarket notification filed by Nobles Medical Technologies Ii, Inc. with the FDA for Noblestitch El Noblestitch Mr Noblestitch Ta.
Device ID | K113494 |
510k Number | K113494 |
Device Name: | NOBLESTITCH EL NOBLESTITCH MR NOBLESTITCH TA |
Classification | Suture, Nonabsorbable, Synthetic, Polypropylene |
Applicant | NOBLES MEDICAL TECHNOLOGIES II, INC. 17080 Newhope St Fountain Valley, CA 92708 |
Contact | Maria Hategan |
Correspondent | Maria Hategan NOBLES MEDICAL TECHNOLOGIES II, INC. 17080 Newhope St Fountain Valley, CA 92708 |
Product Code | GAW |
CFR Regulation Number | 878.5010 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-11-25 |
Decision Date | 2012-04-19 |
Summary: | summary |