OSTEO COMPRESSION HIP SCREW— 510(k) K920037

Substantially Equivalent

Osteo AG

FDA 510(k) clearance K920037 for OSTEO COMPRESSION HIP SCREW, Substantially Equivalent on 1992-03-11. Applicant: Osteo AG. Device class: 2.

Clearance details

Applicant
Osteo AG
Product code
Code HRC
Device class
Class 2
Regulation
21 CFR 886.5928
Advisory panel
Ophthalmic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Greenwood, SC, US
Download summary PDFView on FDA.gov ↗

More clearances from Osteo AG

view all

Data sourced from openFDA. This site is unofficial and independent of the FDA.