The following data is part of a premarket notification filed by O'tec Corp. with the FDA for Broad Self-compressing Plate.
Device ID | K905355 |
510k Number | K905355 |
Device Name: | BROAD SELF-COMPRESSING PLATE |
Classification | Plate, Fixation, Bone |
Applicant | O'TEC CORP. 6685 QUINCE SUITE 106 Memphis, TN 38119 |
Contact | Ricardo Heros |
Correspondent | Ricardo Heros O'TEC CORP. 6685 QUINCE SUITE 106 Memphis, TN 38119 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent For Some Indications (SN) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-11-28 |
Decision Date | 1991-01-04 |