Clearance Summary
PIPELINE TOTAL HIP SYSTEM (LINE EXTENSION) received FDA 510(k) clearance under submission number K132626, sponsored by Pipeline Biotechnology. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2013-09-19.
- Submission: K132626
- Applicant / Sponsor: Pipeline Biotechnology
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3358
- Decision date: 2013-09-19
Classification & Regulation
This clearance is catalogued under FDA product code LPH and 21 CFR 888.3358, within the Orthopedic review panel as a Class II device.