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FDA 510(k)

ACID ETCHED LAG SCREWS

K-Number: K070955 · 2007-10-12

ApplicantBiomet Orthopedics, Inc.
Decision Date2007-10-12
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACID ETCHED LAG SCREWS is the device name listed in this FDA 510(k) record. The listed applicant is Biomet Orthopedics, Inc.. It received FDA 510(k) clearance on 2007-10-12 under 510(k) number K070955. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACID ETCHED LAG SCREWS?

ACID ETCHED LAG SCREWS is a medical device that received FDA 510(k) clearance on 2007-10-12. The listed applicant is Biomet Orthopedics, Inc.. The 510(k) number is K070955.

When did ACID ETCHED LAG SCREWS receive FDA 510(k) clearance?

ACID ETCHED LAG SCREWS received FDA 510(k) clearance on 2007-10-12, under 510(k) number K070955.

Who is the listed applicant for ACID ETCHED LAG SCREWS?

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

What is the FDA product code for ACID ETCHED LAG SCREWS?

The FDA product code for ACID ETCHED LAG SCREWS is HSB.

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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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