Cruxi research & evidence
FDA 510(k) Submission Services evidence guides — page 26
Compare documented facts, dated analyses and evidence that can change your project scope. Confirm applicability with a specialist.
Compare FDA 510(k) Submission Services providers- Avenger Radial Head System (K212872): indications, design and recorded evidenceRegulatory decision evidence
- Aventus Thrombectomy System (K251189): indications, design and recorded evidenceRegulatory decision evidence
- Aventus Thrombectomy System (K253925): indications, design and recorded evidenceRegulatory decision evidence
- Aventus Thrombectomy System (K262030): indications, design and recorded evidenceRegulatory decision evidence
- Aveta System 2.0 (K223813): indications, design and recorded evidenceRegulatory decision evidence
- Aveta System, Aveta Disposable Hysteroscope (Pearl/Opal/Coral), Aveta Disposable Cystoscope (Coral) (K213171): indications, design and recorded evidenceRegulatory decision evidence
- Avitus® DragonWing Large Volume Autograft Delivery System (K231456): indications, design and recorded evidenceRegulatory decision evidence
- Avitus® Precision Autograft Delivery System (K230492): indications, design and recorded evidenceRegulatory decision evidence
- AxCess® Expandable Interbody System (K243739): indications, design and recorded evidenceRegulatory decision evidence
- AxTiHA Stand-Alone ALIF System (K212967): indications, design and recorded evidenceRegulatory decision evidence
- Axeo 3 Patient Monitor (K153079): indications, design and recorded evidenceRegulatory decision evidence
- B-Capta (K202154): indications, design and recorded evidenceRegulatory decision evidence
- B4C System (K201989): indications, design and recorded evidenceRegulatory decision evidence
- BA310 Abutment, BIA310 Implant/Abutment (K182116): indications, design and recorded evidenceRegulatory decision evidence
- BAC (K254131): indications, design and recorded evidenceRegulatory decision evidence
- BACT/ALERT MP Reagent System (K190405): indications, design and recorded evidenceRegulatory decision evidence
- BARD PTV DILATATION CATHETER (K122367): indications, design and recorded evidenceRegulatory decision evidence
- BASHIR Endovascular Catheter Ref. No. 7201, BASHIR S-B Endovascular Catheter, Ref. No. 7101 (K222095): indications, design and recorded evidenceRegulatory decision evidence
- BASIC AND DOMINANT FLEX SUCTION PUMPS (K130123): indications, design and recorded evidenceRegulatory decision evidence
- BB Base 3D printing resin for denture base (K191591): indications, design and recorded evidenceRegulatory decision evidence
- BBX-PET Scanner (K210450): indications, design and recorded evidenceRegulatory decision evidence
- BC-5D Hematology Control (K160606): indications, design and recorded evidenceRegulatory decision evidence
- BCM2-Body Composition Monitor (K250634): indications, design and recorded evidenceRegulatory decision evidence
- BD AutoShield Duo Pen Needle (K223286): indications, design and recorded evidenceRegulatory decision evidence
- BD BACTEC FXI Culture System (K260213): indications, design and recorded evidenceRegulatory decision evidence
Page 26 of 228