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Reform Pedicle Screw System
PRECISION SPINE, INC. · Model 39-RD-0502 · UDI-DI 00840019928526
HTE
Prescription
0
510(k) clearances
138
Adverse events (1 deaths)
3
Recalls
175
Facilities
Description
Laminar Elevator, Medium
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-09-24 | SpineFrontier, Inc. | Handles and heads may not be compatible. |
| 2013-09-24 | SpineFrontier, Inc. | Handles and heads may not be compatible. |
| 2013-09-24 | SpineFrontier, Inc. | Handles and heads may not be compatible. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.