Cement Extractor Drill
FDA 510(k) K770204 · Depuy, Inc.
510(k) numberK770204
Submission
- Device name
- Cement Extractor Drill
- Applicant
- Depuy, Inc.
Mchenry, IL, US - Received
- January 31, 1977
- Decision date
- February 8, 1977
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- HXY – Brace, Drill
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 888.4540
- Specialty
- Orthopedic
Other 510(k)s with product code HXY
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|---|---|---|---|
| K923776 | Benderev Drill GuideHXY · Traditional | Neimark Labs, Inc. | 11/06/1992SE |
| K892904 | Mitek Drill GuideHXY · Traditional | Mitek Surgical Products, Inc. | 09/28/1989SE |
| K880264 | Bone Suture Fixation DeviceHXY · Traditional | Orthopedic Systems, Inc. | 03/23/1988SN |
| K880381 | Telos Distal Targeting DeviceHXY · Traditional | Austin Assoc. | 03/15/1988SE |
| K880046 | Hasting Finger Fixator InstrumentsHXY · Traditional | Buckman Co., Inc. | 02/16/1988SE |
| K831043 | Andrews Remote Chuck DrillHXY · Traditional | Orthopedic Systems, Inc. | 04/28/1983SE |
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Questions and answers
When was Cement Extractor Drill cleared by the FDA?
Cement Extractor Drill (K770204) received a 510(k) decision of Substantially Equivalent on February 8, 1977, 8 days after the submission was received.
What is the product code of K770204?
The FDA product code is HXY – Brace, Drill, a Class I (low risk) device regulated under 21 CFR 888.4540.