The following data is part of a premarket notification filed by Limacorporate S.p.a. with the FDA for Limacorporate Smr Cta Humeral Heads.
Device ID | K131112 |
510k Number | K131112 |
Device Name: | LIMACORPORATE SMR CTA HUMERAL HEADS |
Classification | Prosthesis, Shoulder, Semi-constrained, Metal/polymer Cemented |
Applicant | LIMACORPORATE S.P.A. P.O. BOX 696 Winona Lake, IN 46590 -696 |
Contact | Cheryl Hastings |
Correspondent | Cheryl Hastings LIMACORPORATE S.P.A. P.O. BOX 696 Winona Lake, IN 46590 -696 |
Product Code | KWS |
CFR Regulation Number | 888.3660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-04-22 |
Decision Date | 2013-06-07 |
Summary: | summary |