510(k) K171703
K171703 is an FDA 510(k) premarket notification submitted by Panther Orthopedics, Inc. for the device "PUMA System". The FDA issued a decision of Substantially Equivalent on Mar 1, 2018. The device falls under product code HTN (Washer, Bolt Nut), a Class II device regulated under 21 CFR 888.3030.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Mar 1, 2018
- Date Received
- Jun 8, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Washer, Bolt Nut
- Device Class
- Class II
- Regulation Number
- 888.3030
- Review Panel
- OR
- Submission Type
- 510(k)