FDA 510(k)
FDA class 2
Substantially Equivalent
🇫🇷 France
MODIFICATION TO: BIOSORB RESORBABLE VOID FILLER
K Number: K071155
·
Decision Jul 3, 2007
Classifications
1
FEI Numbers
229
Registration Numbers
229
Same Product Code
491
Applicant Total
6
Review Days
69
Research this 510(k) in seconds
The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- MODIFICATION TO: BIOSORB RESORBABLE VOID FILLER
- K Number
- K071155
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3045
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Science For Biomaterials
- Date Received
- April 25, 2007
- Decision Date
- July 3, 2007
- Product Code
- MQV
- Advisory Committee
- Orthopedic
- Review Advisory Committee
- OR
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| MQV | Filler, Bone Void, Calcium Compound | FDA class 2 | Orthopedic |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (MQV), ordered by most recent decision date.
Device 300419 Strip
FDA 510(k)
FDA Class 2
·Orthopedic
JAZBI Resorbable Bone Void Filler
FDA 510(k)
FDA Class 2
·Orthopedic
Vitoss® BiModal Bioactive Bone Graft Substitute Foam Strip; Vitoss® BiModal Bioactive Bone Graft Substitute; Vitoss BBTrauma® Bioactive Bone Graft Substitute; Vitoss® BA2X Bioactive Bone Graft Substitute; Vitoss® Bioactive Foam Bone Graft Substitute Pack; Vitoss® Bioactive Foam Bone Graft Substitute; Vitoss® Foam Bone Graft Substitute; Vitoss® Bone Graft Substitute Filled Canister; Vitoss® Bone Graft Substitute
FDA 510(k)
FDA Class 2
·Orthopedic
Adaptos®Fuse Bone Graft
FDA 510(k)
FDA Class 2
·Orthopedic
FIBERGRAFT BG Putty GPS Bone Graft Substitute FIBERGRAFT BG Putty Bone Graft Substitute FIBERGRAFT AERIDYAN Matrix Bone Graft Substitute FIBERGRAFT BG Matrix Bone Graft Substitute
FDA 510(k)
FDA Class 2
·Orthopedic
Mg OSTEOINJECT; Mg OSTEOREVIVE; Mg OSTEOCRETE
FDA 510(k)
FDA Class 2
·Orthopedic
Other Clearances by Science For Biomaterials
| K Number | Device Name | ||
|---|---|---|---|
| K140226 | OTIS-C-PLUS, NEOTIS PLATE, SCREW 06.5 | Jun 3, 2014 | Substantially Equivalent |
| K120818 | OTIS-C PLUS | Apr 19, 2012 | Substantially Equivalent |
| K090994 | LIGAFIX INTERFACE SCREW | May 6, 2009 | Substantially Equivalent |
| K070507 | MODIFICATION TO: LIGAFIX INTERFERENCE SCREW | Mar 29, 2007 | Substantially Equivalent |
| K061022 | BIO 1-KIT BIOSORB FILLED CARTRIDGE | May 24, 2006 | Substantially Equivalent |