JointPoint
System, Image Processing, Radiological
JOINTPOINT, INC.
The following data is part of a premarket notification filed by Jointpoint, Inc. with the FDA for Jointpoint.
Pre-market Notification Details
| Device ID | K160284 |
| 510k Number | K160284 |
| Device Name: | JointPoint |
| Classification | System, Image Processing, Radiological |
| Applicant | JOINTPOINT, INC. 402 BUTTONWOOD LANE Largo, FL 33770 |
| Contact | Noah D. Wollowick |
| Correspondent | Michelle Mcdonough MUSCULOSKELETAL CLINICAL REGULATORY ADVISERS LLC 1331 H STREET, NW, 12TH FLOOR Washington, DC 20005 |
| Product Code | LLZ |
| CFR Regulation Number | 892.2050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-02-03 |
| Decision Date | 2016-08-03 |
| Summary: | summary |
NIH GUDID Devices
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10603295532040 | K160284 | 000 |
| 10603295522850 | K160284 | 000 |
Trademark Results [JointPoint]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 JOINTPOINT 87280063 5376670 Live/Registered |
DEPUY SYNTHES, INC. 2016-12-23 |
 JOINTPOINT 85931835 not registered Dead/Abandoned |
JointPoint, Inc. 2013-05-14 |
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