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FDA 510(k)

GRIND NO MORE

K-Number: K082301 · 2008-10-06

ApplicantPlacontrol, Inc.
Decision Date2008-10-06
Product CodeOBR
DecisionSubstantially Equivalent

Device Summary

GRIND NO MORE is the device name listed in this FDA 510(k) record. The listed applicant is Placontrol, Inc.. It received FDA 510(k) clearance on 2008-10-06 under 510(k) number K082301. The device is classified under product code OBR. Product code OBR falls under the category of Orthopedic, which includes orthopedic implants, fixation devices, and surgical instruments. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRIND NO MORE?

GRIND NO MORE is a medical device that received FDA 510(k) clearance on 2008-10-06. The listed applicant is Placontrol, Inc.. The 510(k) number is K082301.

When did GRIND NO MORE receive FDA 510(k) clearance?

GRIND NO MORE received FDA 510(k) clearance on 2008-10-06, under 510(k) number K082301.

Who is the listed applicant for GRIND NO MORE?

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

What is the FDA product code for GRIND NO MORE?

The FDA product code for GRIND NO MORE is OBR. This falls under the Orthopedic category.

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Related Devices (Code: OBR)

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.

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Official Source

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

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