Synergy Orthopaedics Intl., Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
S.A.F. Acetabular Cup With Porous Coating Ref K896614
Regimes: 510(k) Registry: 510(k)S.A.F. Acetabular Cup Ref K895157
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Synergy Orthopaedics Intl., Inc. have in the registry?
The registry currently lists 2 devices for Synergy Orthopaedics Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Synergy Orthopaedics Intl., Inc.'s devices?
Among its 2 most recently registered devices, Synergy Orthopaedics Intl., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Synergy Orthopaedics Intl., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Synergy Orthopaedics Intl., Inc.'s devices are Class III. Each device page shows its own class and authorisation.
What are the newest devices from Synergy Orthopaedics Intl., Inc. in the registry?
The most recently registered devices listed for Synergy Orthopaedics Intl., Inc. include S.A.F. ACETABULAR CUP WITH POROUS COATING and S.A.F. ACETABULAR CUP.