1
/
of
0
FDA 510(k), K071176, MODIFICATION TO: ARTHREX INTERFERENCE SCREW
FDA 510(k), K071176, MODIFICATION TO: ARTHREX INTERFERENCE SCREW
Regular price
$89.00 USD
Regular price
Sale price
$89.00 USD
Unit price
/
per
510(K) Number: K071176
Device Name: MODIFICATION TO: ARTHREX INTERFERENCE SCREW
Manufacturer: ARTHREX, INC.
Device Classification Name: Fastener, Fixation, Biodegradable, Soft Tissue
Regulation Number: 888.3030
Classification Product Code: MAI
Date Received: 04/27/2007
Decision Date: 08/03/2007
Regulation Medical Specialty: Orthopedic
Device Name: MODIFICATION TO: ARTHREX INTERFERENCE SCREW
Manufacturer: ARTHREX, INC.
Device Classification Name: Fastener, Fixation, Biodegradable, Soft Tissue
Regulation Number: 888.3030
Classification Product Code: MAI
Date Received: 04/27/2007
Decision Date: 08/03/2007
Regulation Medical Specialty: Orthopedic
Couldn't load pickup availability
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
View full details