The following data is part of a premarket notification filed by Biomedical Ent., Inc. with the FDA for Memograph Staple, Warm System.
Device ID | K993714 |
510k Number | K993714 |
Device Name: | MEMOGRAPH STAPLE, WARM SYSTEM |
Classification | Staple, Fixation, Bone |
Applicant | BIOMEDICAL ENT., INC. 14785 OMICRON DR., SUITE 205 San Antonio, TX 78245 |
Contact | W. Casey Fox |
Correspondent | W. Casey Fox BIOMEDICAL ENT., INC. 14785 OMICRON DR., SUITE 205 San Antonio, TX 78245 |
Product Code | JDR |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-11-02 |
Decision Date | 2000-02-25 |
Summary: | summary |