FDA UDI In Commercial Distribution 🇺🇸 United States

RESTORIS

DI: 00848486008451 · Model: 186005-15 · MAKO SURGICAL CORP.
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RESTORIS
Primary DI
00848486008451
Version / Model
186005-15
Catalog Number
186005-15
Company Name
MAKO SURGICAL CORP.
Labeler DUNS
175239677
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
4
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
84f0852f-0fe6-4257-b44f-782c1b9e07f3

Device Description

Bone Screw

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OQG Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented
OQH Hip, semi-constrained, cemented, metal/polymer + additive, cemented
LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
JDI Prosthesis, hip, semi-constrained, metal/polymer, cemented

GMDN Terms

Code Name
46646 Orthopaedic bone screw, non-bioabsorbable, sterile

Identifiers

Type ID
Primary 00848486008451

Premarket Submissions

Submission Number Supplement Number
K112802 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Diameter: 6.5 Millimeter
Length 15.0 Millimeter