Implantech Conform Binder Submalar Implant
FDA 510(k) K973502 · Implantech Associates, Inc.
510(k) numberK973502
Submission
- Device name
- Implantech Conform Binder Submalar Implant
- Applicant
- Implantech Associates, Inc.
Washington, DC, US - Received
- September 16, 1997
- Decision date
- November 7, 1997
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- LZK – Implant, Malar
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.3550
- Specialty
- General, Plastic Surgery
- Implant
- Yes
Other 510(k)s with product code LZK
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K021419 | Aart Malar ImplantLZK · Traditional | Aesthetic and Reconstructive Technologies, Inc. | 07/02/2002SE |
| K002886 | Implantech Composite Facial Implants (Malar, Chin, and Nasal)LZK · Traditional | Implantech Associates, Inc. | 11/24/2000SE |
| K992240 | Pillar Malar ImplantLZK · Traditional | Pillar Surgical, Inc. | 11/22/1999SE |
| K983756 | Surgiform Anatomical MalarLZK · Special | Surgical Technology Laboratories, Inc. | 11/20/1998SE |
| K982763 | Seare Biomedical Malar ImplantsLZK · Traditional | Seare Biomedical Corp. | 09/30/1998SE |
| K981835 | Silimed Malar ImplantLZK · Traditional | Silimed, LLC | 07/09/1998SE |
| K980141 | Spectrum Designs Projection Malar ImplantLZK · Traditional | Spectrum Designs, Inc. | 03/03/1998SE |
| K980140 | Spectrum Designs Medial Malar ImplantLZK · Traditional | Spectrum Designs, Inc. | 03/03/1998SE |
| K980139 | Spectrum Designs Profile Malar ImplantLZK · Traditional | Spectrum Designs, Inc. | 03/03/1998SE |
| K973574 | Duralastic Anatomical Malar ImplantLZK · Traditional | Hanson Medical, Inc. | 10/24/1997SE |
More from Hanson Medical, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K200610 | Customized Contour ImplantFWP · Traditional | 12/23/2020SE |
| K191130 | Customized Contour ImplantFWP · Traditional | 08/23/2019SE |
| K172389 | ePTFE-Coated Auricular ImplantFZD · Traditional | 07/18/2018SE |
| K141027 | 3D Eptfe; Anatomical Chin, Curvilinear Chin, Extended Anatomical Chin Implant, Submalar…FWP · Traditional | 07/10/2014SE |
| K071470 | Implantech Eptfe Sheeting, Model Eptfe-XxxFTL · Traditional | 08/31/2007SE |
| K052505 | Calf Implant, Model EC17-XMIB · Traditional | 11/04/2005SE |
| K052504 | Gluteal Implant, Models RND 5-X, TRD 6-XMIB · Traditional | 11/04/2005SE |
| K013732 | GelzoneMDA · Traditional | 02/07/2002SE |
| K012419 | Conform Sheeting, Model IgelMDA · Traditional | 10/24/2001SE |
| K002886 | Implantech Composite Facial Implants (Malar, Chin, and Nasal)LZK · Traditional | 11/24/2000SE |
Questions and answers
When was Implantech Conform Binder Submalar Implant cleared by the FDA?
Implantech Conform Binder Submalar Implant (K973502) received a 510(k) decision of Substantially Equivalent on November 7, 1997, 52 days after the submission was received.
What is the product code of K973502?
The FDA product code is LZK – Implant, Malar, a Class II (moderate risk) device regulated under 21 CFR 878.3550.