The following data is part of a premarket notification filed by R&r Medical, Inc. with the FDA for Stealth Fusion System, Model Rr 1000.
Device ID | K043174 |
510k Number | K043174 |
Device Name: | STEALTH FUSION SYSTEM, MODEL RR 1000 |
Classification | Appliance, Fixation, Nail/blade/plate Combination, Multiple Component |
Applicant | R&R MEDICAL, INC. 1001 OAKWOOD BLVD Round Rock, TX 78681 |
Contact | Jd Webb |
Correspondent | Jd Webb R&R MEDICAL, INC. 1001 OAKWOOD BLVD Round Rock, TX 78681 |
Product Code | KTT |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-11-16 |
Decision Date | 2005-02-07 |
Summary: | summary |