Femoral elevator for DAA 9095.11.102

GUDID 08033390093910

Femoral elevator for DAA

LIMACORPORATE SPA

Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable

Primary Device ID	08033390093910
NIH Device Record Key	c2670518-25ba-4a11-93a5-802284fa20c7
Commercial Distribution Discontinuation	2022-01-04
Commercial Distribution Status	Not in Commercial Distribution
Brand Name	Femoral elevator for DAA
Version Model Number	Femoral elevator
Catalog Number	9095.11.102
Company DUNS	432066322
Company Name	LIMACORPORATE SPA
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08033390093910 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K112898

FDA Product Code

LPH	Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented