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Instruments Designed For Press-Fit Osteochondral Implants

FDA product code QBO · 2 cleared devices

Class 2 Orthopedic
Regulation
21 CFR 888.4505
Review panel
OR
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
2018-06-20 – 2019-09-04

The device is intended to manipulate bone and cartilage tissue or implant materials for the positioning, alignment, defect creation, or placement of press-fit osteochondral implants.

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