Home › Device types › HWD
Starter, Bone Screw
FDA product code HWD · Class 1 · Orthopedic
225
Registered devices
28
Adverse events
1
Recalls
0
510(k) clearances
Devices with this code
Specials — Seaspine Orthopedics CorporationPower Dental U.S.A., Inc. — Power Dental U.S.A. Inc.Dakota ALIF Plate System — PRECISION SPINE, INC.INBONE — WRIGHT MEDICAL TECHNOLOGY, INC.Power Dental USA — Power Dental U.S.A. Inc.Made-To-Order — WRIGHT MEDICAL TECHNOLOGY, INC.S³SHOULDER NAIL PLATE LOCK SCREW — Biomet Orthopedics, LLCMariner — Seaspine Orthopedics CorporationAtoll — Seaspine Orthopedics CorporationPower Dental USA — Power Dental U.S.A. Inc.Power Dental USA — Power Dental U.S.A. Inc.Power Dental USA — Power Dental U.S.A. Inc.Power Dental USA — Power Dental U.S.A. Inc.AMP-LTX — ALPHATEC SPINE, INC.DISTAL TIBIA HANDLE SET SCREW — Biomet Orthopedics, LLCUniversal2 Total Wrist Implant System — Smith & Nephew, Inc.NA — SYNTHES (U.S.A.) LPTIBIAXYS® — NEWDEALPower Dental U.S.A., Inc. — Power Dental U.S.A. Inc.Power Dental USA — Power Dental U.S.A. Inc.Power Dental USA — Power Dental U.S.A. Inc.Power Dental USA — Power Dental U.S.A. Inc.Power Dental USA — Power Dental U.S.A. Inc.NexGen Anterior Cervical Plate System — PRECISION SPINE, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2011-03-10 | Biomet, Inc. | One lot of 30 mm screws was switched with one lot of 25 mm screws. |
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