The following data is part of a premarket notification filed by Osteo Ag with the FDA for Osteo Kirschner Wire.
Device ID | K922193 |
510k Number | K922193 |
Device Name: | OSTEO KIRSCHNER WIRE |
Classification | Pin, Fixation, Smooth |
Applicant | OSTEO AG 208 WILSON BRIDGE RD. Greenwood, SC 29646 |
Contact | Bryson, Jr. |
Correspondent | Bryson, Jr. OSTEO AG 208 WILSON BRIDGE RD. Greenwood, SC 29646 |
Product Code | HTY |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-05-11 |
Decision Date | 1992-07-23 |