FDA UDI Not in Commercial Distribution 🇺🇸 United States

Ascension®

DI: 10381780235057 · Model: PYROMCPINSTP · Ascension Orthopedics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Ascension®
Primary DI
10381780235057
Version / Model
PYROMCPINSTP
Company Name
Ascension Orthopedics, Inc.
Labeler DUNS
942377524
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-15
Public Version
4
Public Version Date
2023-05-02
Public Version Status
Update
Public Device Record Key
4d4ced5a-7882-4da8-b7b3-0a09d255ac9c
Distribution End Date
2023-03-31

Device Description

The Ascension MCP is indicated for use as a total joint replacement of index, long, ring, and small finger metacarpophalangeal (MCP) joints that exhibit symptoms of pain, limited motion, or inadequate bony alignment secondary to articular destruction or degenerative disease related to rheumatoid arthritis, systemic lupus erythematosus, osteoarthritis, or post-traumatic arthritis where soft tissue reconstruction can provide adequate stabilization. The set includes proximal trials, distal trials, and silicone trials to evaluate the size and fit of the appropriate implant. Instruments are included to assist with the trials.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
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
KYJ PROSTHESIS, FINGER, CONSTRAINED, POLYMER

GMDN Terms

Code Name
44758 General external orthopaedic fixation system implantation kit, reusable

Identifiers

Type ID
Secondary M268PYROMCPINSTP1
Primary 10381780235057

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K022892 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 21.7 in L x 10.0 in W x 2.4 in H