Ldr Spine USA, Inc.
INTERBRIDGE INTERSPINOUS POSTERIOR FIXATION SYSTEM
SKU K133363UPC PEK
In Stock
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IIFDA 510(k) Cleared (K133363)
1
Free shipping on orders over $99 · 30-day returns
Ldr Spine USA, Inc.
Free shipping on orders over $99 · 30-day returns
INTERBRIDGE INTERSPINOUS POSTERIOR FIXATION SYSTEM is an FDA 510(k)-cleared medical device (K133363) manufactured by Ldr Spine USA, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 6, 2014. Regulation: 8.
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