Medical Device Manufacturer · US , Alexandria , VA

Pipeline Orthopedics - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2012
9
Total
9
Cleared
0
Denied

Pipeline Orthopedics has 9 FDA 510(k) cleared medical devices. Based in Alexandria, US.

Historical record: 9 cleared submissions from 2012 to 2013. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Pipeline Orthopedics Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Pipeline Orthopedics
9 devices
1-9 of 9
Cleared Oct 03, 2013
NEO KNEE SYSTEM
K131368 · JWH
Orthopedic · 143d
Cleared Sep 23, 2013
PIPELINE KNEE SYSTEM
K132046 · JWH
Orthopedic · 83d
Cleared Jul 01, 2013
PIPELINE TOTAL HIP SYSTEM (LINE EXTENSION)
K130353 · LPH
Orthopedic · 139d
Cleared Jun 13, 2013
PIPELINE TOTAL HIP SYSTEM
K131237 · LPH
Orthopedic · 43d
Cleared May 24, 2013
PIPELINE KNEE SYSTEM
K123692 · JWH
Orthopedic · 172d
Cleared May 03, 2013
NEO PS KNEE SYSTEM
K122500 · JWH
Orthopedic · 260d
Cleared Apr 20, 2012
NEO CR KNEE SYSTEM
K120313 · JWH
Orthopedic · 79d
Cleared Mar 20, 2012
PIPELINE CR PRIMARY KNEE SYSTEM
K113122 · JWH
Orthopedic · 151d
Cleared Mar 09, 2012
PIPELINE TOTAL HIP SYSTEM
K112802 · OQG
Orthopedic · 164d
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