FDA UDI In Commercial Distribution 🇺🇸 United States

SPIRA-A

DI: B030SPA1020390 · Model: SPA-102-039 · CAMBER SPINE TECHNOLOGIES, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SPIRA-A
Primary DI
B030SPA1020390
Version / Model
SPA-102-039
Company Name
CAMBER SPINE TECHNOLOGIES, LLC
Labeler DUNS
054205979
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-26
Public Version
1
Public Version Date
2023-11-03
Public Version Status
New
Public Device Record Key
ec6eb32b-d31f-4ff7-bbd4-6e087ec54df1

Device Description

Trial, 30 x 38mm, 20° Lordotic, 15mm

Device Characteristics

Single Use
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Primary B030SPA1020390

Customer Contacts