KDG · Class I · 21 CFR 878.4820

FDA Product Code KDG: Chisel (osteotome)

Leading manufacturers include Edward Weck, Inc..

11
Total
11
Cleared
49d
Avg days
1978
Since

FDA 510(k) Cleared Chisel (osteotome) Devices (Product Code KDG)

11 devices
1–11 of 11
Cleared Mar 09, 1978
ANDERSON-NEIVERT OSTEOTOME
K772373
Edward Weck, Inc.
General & Plastic Surgery · 72d
Cleared Mar 09, 1978
SILVER OSTEOTOME
K772374
Edward Weck, Inc.
General & Plastic Surgery · 72d
Cleared Mar 09, 1978
NEIVERT OSTEOTOME
K772376
Edward Weck, Inc.
General & Plastic Surgery · 72d

About Product Code KDG - Regulatory Context