Centering Plug
FDA 510(k) K900392 · Allo Pro Corp.
510(k) numberK900392
Submission
- Device name
- Centering Plug
- Applicant
- Allo Pro Corp.
Clearwater, FL, US - Received
- January 26, 1990
- Decision date
- March 1, 1990
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- LZN – Cement Obturator
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.3300
- Specialty
- General, Plastic Surgery
- Implant
- Yes
Other 510(k)s with product code LZN
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K220838 | Artisan Bone Plug, Universal Cement RestrictorLZN · Traditional | Howmedica Osteonics, Dba Stryker Orthopaedics | 05/20/2022SE |
| K061824 | Tornier Cement RestrictorLZN · Traditional | Tornier | 09/14/2006SE |
| K032685 | Cemstop Cement RestrictorLZN · Traditional | Teknimed, S.A. | 11/26/2003SE |
| K023680 | Biobuck Cement RestrictorLZN · Special | Smith & Nephew, Inc. | 11/19/2002SE |
| K011943 | Impro Vise Absorbable Cement Flow RestrictorLZN · Traditional | Kensey Nash Corp. | 09/19/2001SE |
| K010840 | SynplugLZN · Special | Isotis NV | 04/20/2001SE |
| K993841 | Cemstop Cement RestrictorLZN · Traditional | Encore Orthopedics, Inc. | 05/04/2000SE |
| K000587 | Shuttle StopLZN · Traditional | Isotis NV | 05/04/2000SE |
| K992462 | Osteonics Universal Distal Cement PlugLZN · Traditional | Howmedica Osteonics Corp. | 08/13/1999SE |
| K972411 | Link Cement PlugLZN · Traditional | Turnkey Intergration USA, Inc. | 08/29/1997SE |
More from Turnkey Intergration USA, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K901581 | GSB ElbowJDC · Traditional | 10/22/1990SE |
| K900425 | Surgical Cotton GlovesLYU · Traditional | 09/07/1990SE |
| K896669 | Weber PermalockLZO · Traditional | 02/06/1990SN |
| K892644 | Biolox Ceramic BallLZO · Traditional | 10/19/1989SE |
| K885049 | Rs-Cup Acetabular ProsthesisKWA · Traditional | 01/13/1989SE |
| K864999 | Kennedy StemJDI · Traditional | 09/09/1987SE |
| K871453 | Zweymueller-Sl Hip Prosthesis StemKWA · Traditional | 07/13/1987SE |
| K851213 | Zweymuller CupKWA · Traditional | 05/28/1985SE |
| K841391 | Weber-Stuhmer Hip Prosthesis StemJDI · Traditional | 04/13/1984SE |
| K830948 | Weber/Stiihmer Femoral Head ProsthesisJDI · Traditional | 07/12/1983SE |
Questions and answers
When was Centering Plug cleared by the FDA?
Centering Plug (K900392) received a 510(k) decision of Substantially Equivalent on March 1, 1990, 34 days after the submission was received.
What is the product code of K900392?
The FDA product code is LZN – Cement Obturator, a Class II (moderate risk) device regulated under 21 CFR 878.3300.