SPECTRUM® GV Bone Cement
FDA 510(k) clearance K231556 · decided 2023-12-20
Clearance details
- K-number
- K231556
- Device name
- SPECTRUM® GV Bone Cement
- Applicant
- Osteoremedies, LLC
- Decision
- Substantially Equivalent
- Date received
- 2023-05-30
- Decision date
- 2023-12-20
- Days to decision
- 204 days
- Clearance type
- Traditional
- Product code
- LOD
- Device class
- 2
- Regulation number
- 888.3027
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Memphis, TN, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Osteoremedies
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
No recalls on record reference this clearance.