Internal Fixation Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Internal Fixation Systems, Inc. makes
Internal Fixation Systems, Inc. manufactures orthopedic hardware for bone stabilization, including cannulated bone screws, subtalar implants, and profile plates, screws, and washers for internal fixation procedures.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The company is based in the United States.
Catalogue
Ifs Cannulated Bone Screw Ref K061620
Regimes: 510(k) Registry: 510(k)Ifs Bone Fixation Devices Ref K071035
Regimes: 510(k) Registry: 510(k)Ifs Subtalar Implant Ref K113399
Regimes: 510(k) Registry: 510(k)Ifs Profile Plates, Screws, And Washers Ref K110086
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Internal Fixation Systems, Inc. have in the registry?
The registry currently lists 4 devices for Internal Fixation Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Internal Fixation Systems, Inc.'s devices?
Among its 4 most recently registered devices, Internal Fixation Systems, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Internal Fixation Systems, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Internal Fixation Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Internal Fixation Systems, Inc. in the registry?
The most recently registered devices listed for Internal Fixation Systems, Inc. include IFS CANNULATED BONE SCREW, IFS BONE FIXATION DEVICES, IFS SUBTALAR IMPLANT and IFS PROFILE PLATES, SCREWS, AND WASHERS.