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
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