Osteotomy Guide Co.
Country not established
- Devices
- 3
What Osteotomy Guide Co. makes
Osteotomy Guide Co. manufactures surgical guides and screws for orthopedic procedures, including the REESE OSTEOTOMY GUIDE SYS, SHORTENING OSTEOTOMY GUIDE, and REESE ARTHRODESIS SCREW.
The company's devices are listed in the FDA 510(k) registry and include Class I and Class II devices. Osteotomy Guide Co. is based in the US.
Catalogue
Reese Osteotomy Guide Sys Ref K841470
Regimes: 510(k) Registry: 510(k)Shortening Osteotomy Guide Ref K861576
Regimes: 510(k) Registry: 510(k)Reese Arthrodesis Screw Ref K860323
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Osteotomy Guide Co. have in the registry?
The registry currently lists 3 devices for Osteotomy Guide Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Osteotomy Guide Co.'s devices?
Among its 3 most recently registered devices, Osteotomy Guide Co. has devices listed in FDA 510(k) (3 devices).
What risk classes do Osteotomy Guide Co.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Osteotomy Guide Co.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Osteotomy Guide Co. in the registry?
The most recently registered devices listed for Osteotomy Guide Co. include REESE OSTEOTOMY GUIDE SYS, SHORTENING OSTEOTOMY GUIDE and REESE ARTHRODESIS SCREW.