Medical Device Manufacturer · US , Rockaway , NJ

LinkBio Corp.

2 submissions · 2 cleared · Since 2019
2
Total
2
Cleared
0
Denied

LinkBio Corp. — FDA 510(k) Submissions

LinkBio Corp. has submitted 2 FDA 510(k) premarket notifications since 2019, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/polymer, Shoulder Arthroplasty Implantation System . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
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