Biomet, Inc.
COMPREHENSIVE SEGMENTAL REVISION SYSTEM (SRS)
SKU K111746UPC KWT
In Stock
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IIFDA 510(k) Cleared (K111746)
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Free shipping on orders over $99 · 30-day returns
Biomet, Inc.
Free shipping on orders over $99 · 30-day returns
COMPREHENSIVE SEGMENTAL REVISION SYSTEM (SRS) is an FDA 510(k)-cleared medical device (K111746) manufactured by Biomet, 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 December 14, 2011. Regulation: 8.
