Cohort Medical Products Group, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Cohort Medical Products Group, Inc. makes
Cohort Medical Products Group, Inc. manufactures orthopedic fixation devices, including bone screws (both standard and cannulated), a spinal retractor system for anterior approaches, and discectomy tools for spinal surgery. Their portfolio also includes an anterior plate system designed for spinal stabilization procedures.
The company’s devices are classified under FDA categories Class I and Class II, with submissions recorded in the FDA’s 510(k) clearance registry. Products are listed under US jurisdiction.
Catalogue
Bone Screw Ref K943804
Regimes: 510(k) Registry: 510(k)Cannulated Bone Screw Ref K943474
Regimes: 510(k) Registry: 510(k)Cohort Avb Retractor System Ref K943472
Regimes: 510(k) Registry: 510(k)Cohort Discectomy Systems (Cds) Ref K964975
Regimes: 510(k) Registry: 510(k)Cohort(Tm) Anterior Plate System (Aps) Ref K950011
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cohort Medical Products Group, Inc. have in the registry?
The registry currently lists 5 devices for Cohort Medical Products Group, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cohort Medical Products Group, Inc.'s devices?
Among its 5 most recently registered devices, Cohort Medical Products Group, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Cohort Medical Products Group, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Cohort Medical Products Group, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cohort Medical Products Group, Inc. in the registry?
The most recently registered devices listed for Cohort Medical Products Group, Inc. include BONE SCREW, CANNULATED BONE SCREW, COHORT AVB RETRACTOR SYSTEM and COHORT DISCECTOMY SYSTEMS (CDS).