TendoNova wins FDA Clearance for Its New Microinvasive Ocelot Surgical Tool
ATLANTA, March 23, 2022 /PRNewswire/ -- TendoNova, an emerging leader in microinvasive sports medicine procedures, is pleased to announce the FDA 510(k) clearance of its new Ocelot surgical tool, which uses an innovative technology for fragmentation or debridement of soft tissue.
- ATLANTA, March 23, 2022 /PRNewswire/ -- TendoNova, an emerging leader in microinvasive sports medicine procedures, is pleased to announce the FDA 510(k) clearance of its new Ocelot surgical tool, which uses an innovative technology for fragmentation or debridement of soft tissue.
- TendoNova plans to manufacture the Ocelot in Georgia and is presently working to validate the Ocelot disposable component production.
- Founded in 2017, TendoNova is a medical device company that is an emerging leader in microinvasive sports medicine procedures.
- The company's initial product is the Ocelot TSD 1000, a patented, FDA cleared medical device for fragmentation or debridement of soft tissue.