510(k) DEN220030— RemeOs™ Screw LAG Solid

Unknown

Bioretec, Ltd.

Clearance details

Applicant
Bioretec, Ltd.
Product code
Code QJD
Advisory panel
Orthopedic
Date received
Decision date
Decision
Unknown
Clearance type
Direct
Location
Tampere, FI
View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.