Fine Osteotomy
K-Number: K240703 · 2024-04-12
ApplicantBodycad Laboratories, Inc.
Decision Date2024-04-12
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Fine Osteotomy is a medical device manufactured by Bodycad Laboratories, Inc.. It received FDA 510(k) clearance on 2024-04-12 under approval number K240703. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Fine Osteotomy?
Fine Osteotomy is a medical device that received FDA 510(k) clearance on 2024-04-12. It is manufactured by Bodycad Laboratories, Inc.. The 510(k) number is K240703.
When was Fine Osteotomy approved by the FDA?
Fine Osteotomy received FDA 510(k) clearance on 2024-04-12, under approval number K240703.
What company makes Fine Osteotomy?
Fine Osteotomy is manufactured by Bodycad Laboratories, Inc..
What is the FDA product code for Fine Osteotomy?
The FDA product code for Fine Osteotomy is HRS.
Other Devices by Bodycad Laboratories, Inc.
Related Devices (Code: HRS)
K163086VLP MINI-MOD 2.0mm Column PlatesSmith & Nephew, Inc.
K162829Medline UNITE® Ankle Fracture Plating SystemMedline Industries, Inc.
K162974Biomet Microfixation RibFix Blu Thoracic Fixation SystemBiomet Microfixation
K163007Biomet Microfixation SternaLock 360 Sternal Closure SystemBiomet Microfixation
K161696aap LOQTEQ® Distal Lateral Humerus Plate 2.7/3.5Aap Implantate AG
K161747LOQTEQ® VA Distal Tibia Plate System: LOQTEQ® VA Distal Medial Tibia Plate 3.5; LOQTEQ® VA Distal Anterolateral Tibia Plate 3.5; LOQTEQ® VA Distal Fibula Plate 2.7/3.5Aap Implantate AG
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.