Biomedical Ent., Inc.
MEMOGRAPH; OSSTAPLE - ORAL AND MAXILLIOFACIAL PROCEDURES FOR THE MEMOGRAPH STAPLE SYSTEM
SKU K001219UPC JEY
In Stock
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IIFDA 510(k) Cleared (K001219)
1
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Biomedical Ent., Inc.
Free shipping on orders over $99 · 30-day returns
MEMOGRAPH; OSSTAPLE - ORAL AND MAXILLIOFACIAL PROCEDURES FOR THE MEMOGRAPH STAPLE SYSTEM is an FDA 510(k)-cleared medical device (K001219) manufactured by Biomedical Ent., Inc.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 20, 2000. Regulation: 8.
