510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K852891Substantially Equivalent

Spinal Fixation Instrumentation System

Buckman Co., Inc., Martinez CA / Traditional, Substantially Equivalent

K852891 is the FDA 510(k) clearance record for SPINAL FIXATION INSTRUMENTATION SYSTEM, cleared for Buckman Co., Inc. on . FDA records list 111 510(k) clearances for Buckman Co., Inc., from to . As of , FDA records show no recalls naming K852891.

Clearance record

Decision date
Received
(17 days to decision)
Review panel
Unknown
Applicant
Buckman Co., Inc. 921 Calle Verde, Martinez CA
Third party review
No