Edward Weck, Inc.
NEIVERT OSTEOTOME
SKU K772376UPC KDG
In Stock
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IFDA 510(k) Cleared (K772376)
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Free shipping on orders over $99 · 30-day returns
Edward Weck, Inc.
Free shipping on orders over $99 · 30-day returns
NEIVERT OSTEOTOME is an FDA 510(k)-cleared medical device (K772376) manufactured by Edward Weck, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 8, 1978. Regulation: 8.
