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FDA 510(k)

IMPLANTECH CONFORM BINDER SUBMALAR IMPLANT

K-Number: K973502 · 1997-11-07

ApplicantImplantech Associates, Inc.
Decision Date1997-11-07
Product CodeLZK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

IMPLANTECH CONFORM BINDER SUBMALAR IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Implantech Associates, Inc.. It received FDA 510(k) clearance on 1997-11-07 under 510(k) number K973502. The device is classified under product code LZK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPLANTECH CONFORM BINDER SUBMALAR IMPLANT?

IMPLANTECH CONFORM BINDER SUBMALAR IMPLANT is a medical device that received FDA 510(k) clearance on 1997-11-07. The listed applicant is Implantech Associates, Inc.. The 510(k) number is K973502.

When did IMPLANTECH CONFORM BINDER SUBMALAR IMPLANT receive FDA 510(k) clearance?

IMPLANTECH CONFORM BINDER SUBMALAR IMPLANT received FDA 510(k) clearance on 1997-11-07, under 510(k) number K973502.

Who is the listed applicant for IMPLANTECH CONFORM BINDER SUBMALAR IMPLANT?

The FDA 510(k) record lists Implantech Associates, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMPLANTECH CONFORM BINDER SUBMALAR IMPLANT?

The FDA product code for IMPLANTECH CONFORM BINDER SUBMALAR IMPLANT is LZK.

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Other records listing Implantech Associates, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K200610Customized Contour ImplantK191130Customized Contour ImplantK172389ePTFE-Coated Auricular ImplantK071470IMPLANTECH EPTFE SHEETING, MODEL EPTFE-XXXK052504GLUTEAL IMPLANT, MODELS RND 5-X, TRD 6-XK052505CALF IMPLANT, MODEL EC17-X

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Related Devices (Code: LZK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K021419AART MALAR IMPLANTAesthetic and Reconstructive Technologies, Inc.K002886IMPLANTECH COMPOSITE FACIAL IMPLANTS (MALAR, CHIN, AND NASAL)Implantech Associates, Inc.K992240PILLAR MALAR IMPLANTPillar Surgical, Inc.K983756SURGIFORM ANATOMICAL MALARSurgical Technology Laboratories, Inc.K982763SEARE BIOMEDICAL MALAR IMPLANTSSeare Biomedical Corp.K981835SILIMED MALAR IMPLANTSilimed, LLC

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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