Medical Device Manufacturer · US , Byron Center , MI

Transcorp, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2010

Recent clearances: TRANSCORP ACIF SYSTEM, TRANSCORP SPINAL ACCESS SYSTEM, TRANSCORP ACIF SYSTEM

View 4 510(k) Devices ↓
4
Total
4
Cleared
0
Denied

FDA 510(k) Regulatory Record - Transcorp, Inc. Orthopedic ✕

4 devices
1-4 of 4
Cleared Jul 05, 2013
TRANSCORP ACIF SYSTEM
K121178 · ODP
Orthopedic · 443d
Cleared Apr 16, 2012
TRANSCORP SPINAL ACCESS SYSTEM
K113352 · HRX
Orthopedic · 154d
Cleared Sep 13, 2010
TRANSCORP ACIF SYSTEM
K092794 · ODP
Orthopedic · 367d
Cleared May 21, 2010
TRANSCORP TRANS-PLATE ANTERIOR CERVICAL PLATE SYSTEM
K092695 · KWQ
Orthopedic · 261d
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