Pectofix, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Pectofix Dynamic Sternal Fixation System (Dsf) Ref K000694
Regimes: 510(k) Registry: 510(k)Pectofix Sternal Repair Wire Ref K003951
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pectofix, Inc. have in the registry?
The registry currently lists 2 devices for Pectofix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pectofix, Inc.'s devices?
Among its 2 most recently registered devices, Pectofix, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Pectofix, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Pectofix, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pectofix, Inc. in the registry?
The most recently registered devices listed for Pectofix, Inc. include PECTOFIX DYNAMIC STERNAL FIXATION SYSTEM (DSF) and PECTOFIX STERNAL REPAIR WIRE.