The following data is part of a premarket notification filed by Gyrus Ent L.l.c. with the FDA for Bojrab Micro-torp, Model 7014-5845.
Device ID | K990601 |
510k Number | K990601 |
Device Name: | BOJRAB MICRO-TORP, MODEL 7014-5845 |
Classification | Replacement, Ossicular Prosthesis, Total |
Applicant | GYRUS ENT L.L.C. 2925 APPLING RD. Bartlett, TN 38133 |
Contact | Alicia Farage |
Correspondent | Alicia Farage GYRUS ENT L.L.C. 2925 APPLING RD. Bartlett, TN 38133 |
Product Code | ETA |
CFR Regulation Number | 874.3495 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-02-24 |
Decision Date | 1999-03-31 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00821925030565 | K990601 | 000 |