Pivot Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Pivot Medical, Inc. makes
Pivot Medical, Inc. makes knotless suture anchors, including the CinchLock Flex Knotless Suture Anchor, CinchLock Knotless Suture Anchor, and NANOTACK Suture Anchor 1.4mm, with or without a flex inserter.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
CinchLock Flex Knotless Suture Anchor Ref K151314
Regimes: 510(k) Registry: 510(k)Nanotack Suture Anchor 1.4mm Ref K110473
Regimes: 510(k) Registry: 510(k)Cinchlock Knotless Suture Anchor Ref K123651
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Nanotack Suture Anchor 1.4mm With Flex Inserter Ref K130351
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pivot Medical, Inc. have in the registry?
The registry currently lists 5 devices for Pivot Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pivot Medical, Inc.'s devices?
Among its 5 most recently registered devices, Pivot Medical, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Pivot Medical, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Pivot Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pivot Medical, Inc. in the registry?
The most recently registered devices listed for Pivot Medical, Inc. include CinchLock Flex Knotless Suture Anchor, NANOTACK SUTURE ANCHOR 1.4MM, CINCHLOCK KNOTLESS SUTURE ANCHOR and CINCHLOCK KNOTLESS SUTURE ANCHOR, NANOTACK SUTURE ANCHOR 1.4MM.