FDA UDI In Commercial Distribution 🇺🇸 United States

THINFLAP SYSTEM 5/PK

DI: 00888233025317 · Model: 91-6804-5PK · BIOMET MICROFIXATION, INC
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
THINFLAP SYSTEM 5/PK
Primary DI
00888233025317
Version / Model
91-6804-5PK
Catalog Number
91-6804-5PK
Company Name
BIOMET MICROFIXATION, INC
Labeler DUNS
046189866
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-18
Public Version
3
Public Version Date
2025-05-30
Public Version Status
Update
Public Device Record Key
6530d23f-0e10-4792-a7e0-85c651d9e0d1

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
No
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
JEY PLATE, BONE
HBW FASTENER, PLATE, CRANIOPLASTY
GXR COVER, BURR HOLE
GWO Plate, cranioplasty, preformed, alterable

GMDN Terms

Code Name
56642 Orthopaedic bone screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary 00888233025317

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K121589 000
K121624 000
K953385 000