RemeOs Screw LAG Solid— 510(k) DEN220030
UnknownBioretec, Ltd.
FDA 510(k) clearance DEN220030 for RemeOs Screw LAG Solid, Unknown on 2023-03-29. Applicant: Bioretec, Ltd.. Device class: 2.
Clearance details
- Applicant
- Bioretec, Ltd.
- Product code
- Code QJD
- Device class
- Class 2
- Regulation
- 21 CFR 888.3041
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Tampere, FI
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Data sourced from openFDA. This site is unofficial and independent of the FDA.