# Pivot Medical

- Location (FDA's records): Sunnyvale, CA
- FDA decisions: 5 (2011–2015): 5 510(k) clearances
- Names in FDA's records: Pivot Medical (3); Pivot Medical, Inc. (2)
- Product codes: MBI (5)
- Predicates its devices cite: 8 (3 its own); citations of its devices by later devices: 5 (3 its own)
- Recalls linked to its devices: 4 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Smith & Nephew Inc., Endoscopy Division: 2 (https://510kreport.com/company/smith-nephew-endoscopy-division)
- Biomet Manufacturing Corp: 1 (https://510kreport.com/company/biomet-manufacturing)
- Biomet Sports Medicine: 1 (https://510kreport.com/company/biomet-sports-medicine)
- Smith & Nephew Endoscopy, Inc.: 1 (https://510kreport.com/company/smith-nephew-endoscopy)

## Firms that cite its devices most
- Smith and Nephew, Inc.: 1 (https://510kreport.com/company/smith-and-nephew)
- Stryker Corp.: 1 (https://510kreport.com/company/stryker)

## Its most-cited devices
- K131769: Cinchlock Knotless Suture Anchor, Nanotack Suture Anchor 1.4MM (2013), cited by 3
- K110473: Nanotack Suture Anchor 1.4MM (2011), cited by 2

## Recent decisions
- K151314: CinchLock Flex Knotless Suture Anchor (Jul 23, 2015)
- K131769: Cinchlock Knotless Suture Anchor, Nanotack Suture Anchor 1.4MM (Oct 7, 2013)
- K130351: Nanotack Suture Anchor 1.4MM with Flex Inserter (Mar 14, 2013)
- K123651: Cinchlock Knotless Suture Anchor (Feb 21, 2013)
- K110473: Nanotack Suture Anchor 1.4MM (May 25, 2011)

Source page: https://510kreport.com/company/pivot-medical