Carricell
510(k) K132868
Carricell is a Class II device made by Etex Corporation, cleared under FDA 510(k) K132868 on 20 Feb 2015, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK132868 | Date20 Feb 2015 | StatusActive |
Official records
- FDA 510(k) database K132868
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- MQV
- Device class
- Class II
- Regulation
- 21 CFR Part 888.3045
- Advisory committee
- Orthopedic
- FDA decision
- SESE Substantially Equivalent
Similar devices
Other devices filed under FDA product code MQV (Filler, Bone Void, Calcium Compound).
- OsteoSelect Demineralized Bone Matrix Putty by Bacterin International, Inc.
- Magnifuse Bone Graft (Cleared as Grafton II EDBM) MQV by MEDTRONIC SOFAMOR DANEK, INC.
- GranOSTM - beta tricalcium phosphate synthetic bone granules by Tcm Associates, Ltd.
- NANOSS BIOACTIVE, NANOSS BIOACTIVE LOADED, AND NANOSS BIOACTIVE LOADED KIT by Pioneer Surgical Technology, Inc.
- Pioneer Surgical Nanoss BVF-E by Pioneer Surgical Technology, Inc.
- CureOs TCP by Linacol Muh Dan Kim Cev Tek Med Ith Ihr San VE Tic
- Eovia Calcium Phosphate Ceramic by Ortho Tec, LLC
- ATLANTIK by Medical Biomat
- Inion BioRestore Biodegradable Bone Graft Substitute by Inion Oy
- CERAMENT BONE VOID FILLER by Bonesupport AB