Product code HTG— Orthopedic
PATELLAR COMPONENT FOR LUBINUS PATELLAR
- Classification name
- Prosthesis, Knee, Hemi-, Patellar Resurfacing, Uncemented
- Device class
- Class 2
- Regulation
- 21 CFR 888.3580
- Advisory panel
- Orthopedic
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code HTG
FDA has cleared devices under product code HTG between 1977 and 1980, filed by 2 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
- 1980
- 1977
Top applicants under product code HTG
Recent clearances under product code HTG
Data sourced from openFDA. This site is unofficial and independent of the FDA.